Supplier Quality Compliance Engineer

15408

San Angelo, Texas

Engineering

BEPC has an open position for a Supplier Quality Compliance Engineer in San Angelo, TX!

JOB DESCRIPTION

Summary/Objective:

The Supplier Quality Compliance Engineer ensures the execution of quality system compliance activities associated with the receipt and acceptance of robust supplier audit responses for identified supplier audit observations. The Supplier Quality Compliance Engineer performs these activities to applicable quality management system standards for fortune 500 Medical Device Companies. The Supplier Quality Compliance Engineer addresses supplier audit responses for suppliers across different industries such as Medical device, Pharmaceutical, Biotechnology, Microbiology and Sterilization Sciences as needed to meet customer requirements.

This individual will be responsible for supporting external inspections of External Manufacturers and Suppliers. They will also be responsible for supporting internal audits of the client’s Compliance program. Supports in the management, tracking to closure of External Manufacturers and Suppliers commitments to mitigation of identified risks. Supports in the completion of Follow Up reports related to the tracking and completion of External Manufacturing commitments taken to mitigate identified risks.

Responsibilities

Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and client procedures and guidelines, this position:

Assists in the development, implementation and continuous improvement of the client’s Compliance program.
Ensures timely mitigation of risks identified through Supplier Audit Program.
Requests and reviews documentation related to Supplier Audit Response for identified audit observations
Assures that related client Compliance Quality Records are updated in a timely manner and are compliant with company procedures and policies.
Ensures timely completion of activities related to training.
Proactively engages with external partners to develop a robust supplier corrective action response.
Issues Follow Up reports in accordance with client procedural requirements.
Identify process improvements related to standard operating procedures and systems to mitigate risk and drive a quality culture.
Complies with policies, procedures, training requirements and company and regulatory rules and norms.
Performs according to the company's quality policy and corporate rules in all business activities with providers and customers within and outside the company.
Escalates abnormalities and business critical information to the client’s Compliance Leadership.
Maintains quality records where applicable per client records retention procedures.
Responsible for ensuring personal and client Company compliance with all Federal, State, local and Company regulations, policies, and procedures.

Other Duties:

Other duties may be assigned as required by BEPC management. Competencies
Expertise on/detailed knowledge of regulatory requirements in the FDA/ISO/Health Authority regulated industry (medical devices or pharmaceutical), with the ability to relate them to business/quality issues.
Excellent prioritization skills
Excellent written and oral communication skills as well as report writing
Strong collaboration and influence skills to partner effectively both internally and externally
Experience in the Medical Device industry or medical field
Able to enter data on spread sheet and database applications
Ability to make the complex clear and easily understood by others
Knowledge of ISO 13485 and 21CFR 820
Quality system auditor qualifications desirable, e.g. ASQ CQA or CBA, ISO 9001/13485 lead auditor
Ability to work in a sometimes stressful fast paced environment

Supervisory Responsibility:

This position is an individual contributor position.

Work Environment:

This job operates in a professional office environment.
This role routinely uses standard office equipment such as laptop computers and smartphones.

Position Type/Expected Hours of Work:

This is a full-time position, and hours of work typically Monday through Friday, 8:00 a.m. to 5:00 p.m. However, agility and quick response time to customer and employee requests may be required at other times to include evening and weekends.
This position works remotely.
Travel This position requires minimal to no travel, e.g. < 5% as required to meet customer & business needs.

Required Education and Experience:

Bachelor’s degree or equivalent required; concentration in Engineering or technical field preferred
5-8 years or more experience in a FDA regulated industry (pharmaceutical or medical devices) or another highly regulated industry is required.

AAP/EEO Statement:

BEPC Inc. policy is to affirmatively implement equal opportunity for all employees and applicants for employment without regard to race, color, religion, sex, national origin, disability, military status, genetic information, or any other basis prohibited by law. Additionally, BEPC Inc. does not discriminate against an employee or applicant who acts to oppose such discrimination or participates in the investigation of a complaint related to discriminatory employment practice. Employment decisions will be made on the basis of each applicant’s job qualifications, experience, and abilities.

BEOCS

Date Added: 10-19-2021

Associate Scientist - Immunology

15407

Billerica, Massachusetts

Other Area(s)

BEPC is looking for a confident Associate Scientist to come join our fast-growing team in Billerica, MA!

Contract W2 period: 6-month contract with possibilities for extensions

Pay: $30.75/hour

Shift: M-F, 9am-5pm

Description:
Associate Scientist, Immunology, EMD Serono
We are seeking a highly motivated BS/MS level scientist to join the Immunology team of EMD Serono located at our Billerica, MA. EMD Serono is the biopharmaceutical division of Merck KGaA, Darmstadt, Germany. We strive to create value and benefit patients by transforming medical science into breakthrough solutions in our core therapeutic areas of neurodegenerative diseases, fertility and metabolic endocrinology, oncology and autoimmune/inflammatory diseases.

Job Responsibilities:
The Associate Scientist will contribute to the discovery of drugs for treating autoimmune diseases. He or she will work collaboratively with a group of scientists to develop and conduct in vitro cell-based assays to further our understanding of human autoimmune diseases and evaluate potential drug candidates. Responsibilities includes:

Develop and conduct cell-based assays using human primary immune cells or cell lines to support target validation, mechanism of action studies and drug discovery efforts
Conduct gene expression or protein analysis
Operate state of the art laboratory equipment such as Flow Cytometer, Luminex, MSD/EnVision plate reader and QPCR-based expression platforms, as needed
Independently analyze and interpret data and trouble-shoot experiments
Record data accurately in Electronic Laboratory Notebook and maintain records per company policy and legal requirements. Prepare study protocols and reports per request
Closely work with members in the Immunology group to support departmental goals

Qualifications:

Bachelors or Masters degree in biology, preferably in Immunology or cell biology
Minimum 1-3 years of practical laboratory experience in Immunology or a related field, pharmaceutical industry experience a plus
Required hands-on experience: Tissue culture/aseptic technique, ELISA, and assay setup including reagent calculations.
Specific knowledge and hands-on experience in the following areas are highly desirable:
Human primary cell culture, immune cell isolation from human whole blood/PBMC
Cell-based assays: proliferation, cytokine assessment
Flow cytometry: multicolor intracellular and surface staining
Molecular Biology: DNA/RNA isolation, QPCR, Western blotting
Bioanalytical assays: ELISA, Luminex, or MSD
Laboratory equipment: FACS, autoMACS, EnVision
Good understanding of basic Immunology principles would be an advantage
Highly proficient with computer software: GraphPad Prism, BD FACS Diva, Flow Jo, Microsoft Office
Needs at least 1 year of research (something outside of just the univ setting).
Cell culture exp
Understand sterile technique
Exp in Elizas (sp) and understand the math, etc..understand assay

BEOCS

Date Added: 10-19-2021

Operator III - 2nd Shift

15401

Menlo Park, California

Manufacturing

BEPC Inc is looking for an Operator III 2^nd shift in Menlo Park CA!
Contract W2 Period: 1 year contract with possibilities for extensions
Pay & Benefits: $24.76/hr. +Medical, Dental, Vision and Life Insurance

*** Shift Hours: 3:00pm – 1:30am ***

We are looking for assemblers to build medical devices according to written instructions. It is necessary to follow the instructions exactly, so we are assessing candidates on whether they follow instructions step by step, and whether they are able to use tools such as screwdrivers, tweezers, and microscopes. They will also meet with a member of our team to discuss their understanding of the importance of quality in manufacturing, the responsibilities of the job, and the candidates' previous experience and background.

Description

This position is responsible for the production of high quality cardiovascular medical devices on a team within a manufacturing cell.
This position includes detailed assembly and operation of various equipment and machinery per documented procedures.
This may include electronic assembly, casting/coating functions, mechanical assembly and packaging.
Cleans tools and equipment per documented procedures.
Disposes hazardous waste material on corresponding hazardous waste areas

Duties

Assembles medical devices and related components.
Depending on work area, it may be a controlled cleanroom environment.
May include use of microscopes, use of hand tools, razor blades, syringes, soldering, adhesive bonding, and operating various equipment.
Performs routine assignments according to specified and/or standardized procedures.
Work is closely and continually reviewed.
Performs visual inspection and precision measurements on components and assemblies.
Performs tests on units using computerized test equipment.
Repairs and corrects devices/components using microscopes and applicable tools.
Packages devices ensuring all parts are accurate and documentation is complete.
Maintains accurate records to ensure travelers, shop floor paperwork and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Follows safety guidelines and utilize appropriate safety devices and equipment when performing all operations.
Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics.
Notifies supervisor or lead of the need to replenish supplies/materials and of any production difficulties that cannot be readily corrected.
Participates with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Cooperates in keeping a clean, sanitary work environment throughout the building.
Performs other related duties as directed or assigned.

Requirements

Must be able to read, comprehend and follow English written procedures at a 6th grade level
Must have good basic math skills at a 6th grade level.
Must be able to speak, follow verbal instructions and communicate effectively in English.
Possesses understanding of and ability to utilize electronic data collection systems and computer software packages.
Must have good dexterity to handle and maneuver small components and parts.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to make critical decisions and judgments with minimal supervision.
High school diploma required
5+ years of experience

BEOCS

Date Added: 10-18-2021

Forklift Driver II - 3rd Shift

15397

Tipp City, Ohio

Manufacturing

Forklift Driver II

15391

Tipp City, Ohio

Manufacturing

Forklift Driver II - 2nd Shift

15390

Tipp City, Ohio

Manufacturing

CW International Release Consultant

15389

Plano, Texas

Other Area(s)

Buyer

15388

Houston, Texas

Other Area(s)

Business Analyst

15386

Scottsdale, Arizona

Other Area(s)

BEPC has Scottsdale AZ 85254 open position for Business Analyst to join our fast-growing team of consultants!

Contract W2 Period: 8 months with possibilities for extension
Pay & Benefits: 41/hr + Medical, Dental, Vision & Life Insurance
Location: 1 DNA Way South San Francisco California, United States

Ref: 15386 - 1033646

Job Description:

Responsible for managing multiple, global technology and telecom provider contracts, services and invoices. Utilizing Microsoft Excel and a variety of database tools for tracking inventory, invoice validation details, and payment of invoices. Researching services (voice, network, and data center) provided by global suppliers. Providing updates and reports to assist Finance and Technology teams with billing reconciliation and inventory. Creating and managing purchase orders (PO) to ensure funding according to budgets and invoice processing against POs for invoice payment. Assist the team with projects as needed.

Requirements:

Strong Microsoft office knowledge including expert level Excel and database tools at intermediate level
Telecom and technology expense management experience
Ability to interpret invoices in various formats including EDI and foreign languages
Project Management and tracking including work effort, financial tracking, work task entries, cost savings, process efficiencies, and quality improvements
Working knowledge of translating contractual commitments to purchase orders, budgets and reconciling to invoices
NetSuite experience preferred, working knowledge of purchase order process and invoice reconciliation required
Exposure to, or working knowledge of expenses related to network, voice, and data centers preferred
Ability to understand and map processes, define and measure process performance and metric trends
Self-motivator with excellent organization skills
Ability to work in a virtual environment, independently, and demonstrate strong leadership skills
Strong analytical, problem-solving, and reporting skills
Must be able to interface with end-user business, technology customers and vendors in an effective and positive manner

Top Skill Set:

Excel and database
Telecom and Technology expense management
Financial tracking / expense management
Netsuite preferred
Financial system
Bachelors preferred

BEPRO

Date Added: 10-18-2021

Packaging Operator - Crew 2

15382

Fairfield, California

Manufacturing

Technical Writer

15381

Scarborough, Maine

Manufacturing

Packaging Operator 1

15379

Sheboygan Falls, Wisconsin

Other Area(s)

BEPC Inc is looking for a Packaging Operator to join our fast growing team of consultants in the Sheboygan Falls, Wisconsin area!

Contract W2 Period: 1 year with possibility of extension

Pay/Benefits: $15/hour

Overtime will be paid at time and a half

Job Description:

Manually and semi-automatically portion chemicals into containers using safety equipment and follow protocols.

ESSENTIAL JOB FUNCTIONS

• Weigh hazardous and non-hazardous chemicals using precision equipment into specific containers. Verify hood and safety equipment function, obtain process order, scan into computer system, verify electronic balance is calibrated

• Verify match of process order and bulk container lot numbers

• Obtain correct type and quantity of containers for process order

• Operate powered pallet and drum movers

• Verify weighed bottles and determine if quantity matches process order requirements

• Pulls samples for customers and/or quality control as required

• Complete paperwork including tray tags, process orders, and computer PKRV scan

• Document process order for specific required data, inclusive of weighing accountability to assure the accuracy of the weighed material using Good Documentation Practices (GDP)

• Fill out data for tray taqs and affix to each tray or case of filled bottles

• Complete production logs

• Maintain equipment, tools, and facilities in safe, clean environment

• Assemble, disassemble semiautomatic powder or liquid dispensing equipment and replace worn or disposable parts as necessary

• Clean semi-automatic dispensing equipment according to manufacturer recommendations and chemical safety protocols

• Clean tools and utensils with appropriate material in hood according to chemical safety protocols

• Clean hood/work station according to method and protocol for specific chemical weighed

• Document cleaning of area/equipment/hood on cleaning log when applicable

• Assemble, test, maintain, and use appropriate safety equipment

• Prepare respiratory protection (check air helmet hoses for leaks, etc., assemble white air helmet)

• Prepare and don Personal Protective Equipment (PPE) as appropriate for weighing protocol

• Clean and maintain reusable safety equipment for next use

• Facilitate packaging operations by providing support for weighers and moving material within the department

• Procures bulk and package components for weighers

• Applies closure and cleans exterior container surface

• Moves materials in department

• Label and overpack bottles of chemicals

• Verify and complete required paperwork and documentation

• Set up, operate, and troubleshoot all automated labeling, sealing, and bagging equipment

• Document all processes on the packaging request. Document all damaged labels. Initial all appropriate processes (data sheets, poly bags, etc.)

• Participates in testing and implementation of changes

• Maintain, clean and keep safe all work areas and equipment following 5S standards

• Take necessary steps to assure we provide our customers with the highest quality product

possible

• Immediately report any situation that could compromise safety or quality

• Miscellaneous duties and tasks as assigned

• Exemplary attendance and adherence to schedule

• Actively participate in a proactive safety culture; identifying hazards, making suggestions for

improvement, coaching coworkers on safety, and working incident free.

BASIC QUALIFICATIONS

Education:

High School Diploma, GED or HSED required

Desirable: High school course work in chemistry or 6 months chemistry related work experience.

Knowledge and Skills:
Read instructions and understand oral and written instructions. Basic math skills including the metric system. Learn SOP's/UOP's, cleaning protocols, work and conduct rules. Learn to use safety equipment. Learn to use semi-automated equipment. Eye-hand coordination. Small/large tool dexterity. Legible handwriting, teamwork, communication skills. Ability to move 50 lbs. Problem solving. Ability to operate a forklift is preferred.

ADDITIONAL LOCAL NEEDS

Environmental Conditions

Packaging/Distribution/Warehouse Environment: Occasionally works near moving mechanical parts.

Is occasionally required to wear appropriate protective gear, (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protection equipment PPE to protect themselves from toxic or corrosive chemicals in the forms of liquids, solids, vapors or airborne particles.

The work area may occasionally be wet, humid, or abnormally hot or cold.

Physical Requirements

If performing packaging duties: While performing the duties of this job, the employee is regularly required to sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch or crawl for long periods of time. The employee must be able to talk, hear, taste and smell. The employee must occasionally lift and/or move up to 50 pounds unassisted and ability to push and pull heavy materials to complete assignment. The employee may be required to lift more poundage with assistance. Specific vision requirements of this job include close vision, distance vision, color vision, peripheral vision, depth vision, and the ability to adjust focus. Regularly uses phones, computers, computer monitors and all office/laboratory equipment. The employee is also required to type at a computer keyboard and have the ability to read CRTs/computer monitors.

If performing packaging/warehouse/distribution duties: While performing the duties of this job, the employee is occasionally required to sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch or crawl for long periods of time. The employee must be able to talk, hear, taste and smell. The employee must occasionally lift and/or move up to 50 pounds unassisted. Employee may be required to move more than 50 pounds with assistance. Specific vision requirements of this job include close vision, distance vision, color vision, peripheral vision, depth vision, and the ability to adjust focus.

Regularly uses phones, computers, computer monitors and all office/laboratory equipment. The employee is also required to type at a computer keyboard and have the ability to read CRTs/computer monitors

BEOCS

Date Added: 10-18-2021

Project Manager, Content Marketing Creative

15377

Newark, New Jersey

Project Management

BEPC is seeking a talented Project Manager, Content Marketing Creative to join our fast-growing team of consultants in Newark, NJ!

W2 Contract Period: 5+ months with possible opportunities for extensions based on business needs and performance.

Pay Rate: $41.63/HR plus we offer Medical, Dental, Vision and Life Insurance benefits after 90 days.

The CM Creative team is looking for a Project Manager to help support the execution of title launch campaigns across a wide variety of digital and traditional platforms. This role is part of the Integrated Marketing team but supports all CM Creative projects.

Be part of a smart and passionate project management-production team that helps the CM Creative team create stunning promotional assets for our top priority programming. In collaboration with the Director, Project Management and Operations, you’ll collaborate with your projects’ creative teams (CDs, ADs, copywriters, designers) and partner with internal stakeholders to produce distinctive, best-in-class campaign launches that attract and convert new customers and engage our existing community of listeners in authentic and compelling ways.

ABOUT YOU:

You’re a skilled project management professional with an obsessive need for order and a background in managing creative projects both internally and with external production partners.
You’re operationally grounded and adept at using data to inform planning and capacity decisions.
You are comfortable speaking your mind and presenting a recommendation with a diplomacy that yields results.
You’re adept at defining and managing tasks, milestones, and multi-month timelines across all aspects of creative development, including the conceptual, pre-production, production, and post-production/delivery phases.
You’re well-versed in digital asset deliverables and delivery workflow for internal and media agency deployment
Your insight and overall demeanor work to build strong rapport and trust with partners across multiple functional areas
You bring together the information, the resources, and the forums to get work done on time and on budget.
You have strong time management skills with the ability to set priorities, multi-task, and meet deadlines in a fast-paced environment.
You are a fast learner and take direction well.

KEY RESPONSIBILITIES

Manage the end-to-end creative development and production lifecycle for mid- and large-scale content-focused marketing campaigns.
Work with the PM Director to review new project requests from internal partners submitted through our project management system for timing and feasibility and to develop comprehensive project plans across a variety of disciplines/platforms.
Lead communication around project status with internal stakeholders. Participate in creative team assignments in collaboration with PM Director, creative directors, and creative VP.
Develop comprehensive milestones and schedules for all assigned projects and work collaboratively with creative and marketing teams (designers, copywriters, creative directors, and strategists) to procure required kickoff information/assets, and communicate project status, deliverables, specs, dependencies, and potential issues.
Work with external production companies and internal partners to execute large scale photo and video shoots: secure photographers and/or directors, negotiate budgets, draft contracts, coordinate talent logistics, and other shoot details
Distill and translate complex information into clear takeaways and actions for the team
Assist in tracking and balancing resource utilization and creative team capacity
Lead regular production and status meetings; generate reports for these meetings
Help the creative team prioritize their work on a daily/weekly basis
Proactively keep team members on deadlines in an effective but positive way

Manage budgets for individual projects: tracking expenses, creating SOWs and POs, and processing invoices. Collaborate with PM director on month-end reporting
Onboard and manage creative agencies and partners as needed
Manage compliance aspects of projects, including talent and footage restrictions, title clearances, music/ footage/ image licensing, talent & location releases, and standards and practices in conjunction with our Legal team.
Quality check final creative as needed, and traffic final assets to stakeholders for campaign execution.
Provide project support to the Director of Project Management and Operations as needed
Provide administrative support to the department as needed, such as managing the schedule and agenda for regular executive reviews
Proactively research and implement new tools and workflows

Qualifications

5+ years project management experience preferably at a TV network, creative agency, or entertainment company
Excellent organizational and project management skills with experience managing multiple projects with competing priorities in a calm and efficient manner.
Experience managing creative development and developing production processes and timelines that support the creative process.
Strong video and photo shoot planning and production experience
Broad project management experience across a variety of media channels, including but not limited to; digital advertising, broadcast, OOH, paid social, organic social, experiential
General knowledge of project management principles, processes, and tools
Strong written and oral communication and presentation skills.
Basic knowledge of video and digital file types
Bachelor's degree or equivalent

Date Added: 10-15-2021

Engineer - Degreed IV

15376

Princeton, New Jersey

Engineering

Packaging Operator 1

15366

Martin, South Carolina

Manufacturing

BEPC Inc is looking for a Packaging Operator to join our fast growing team of consultants in the Martin, South Carolina area!

Contract W2 Period: 1 year with possibility of extension

Pay/Benefits: $16.35/hour

Overtime will be paid at time and a half

Job Description:

2 week rotating schedule: MT (on), WTh (off), FSS (on) and MT (off), WTh (on), FSS (off) 7AM - 7PM

chemical manufacturing experience is preferred.

Support manufacturing of products according to established protocols and perform operations in support of the group, department and company.
ESSENTIAL JOB FUNCTIONS

Perform production operation so Perform packaging operations per current production process and procedures.
Transport chemicals and equipment to and from processes including use of pumps/piping, fork trucks, pallet jacks or dollies.
Ensure quality and quantity of product throughout production process
Wear appropriate PPE for production processes which may include full face respirators, gloves, suit so Clean-up equipment and working areas after production operation so Coordinate appropriate disposal of waste and complete compliance documentation. Communicate and document status of processes, products, and equipment.
Communicate the status of production operations/equipment and bring deviations to the attention of supervisor.
Provide a complete and accurate batch record at the conclusion of production operations consistent with quality guidelines.
Ensure all applicable log books have been filled out completely as required by current procedures Perform operations in compliance with rules and in a safe, orderly manner.
Follow production procedures and safety policies at all time.
Use, clean, and store all personal protective gear appropriately
Label all in-process equipment and containers properly.
Take the necessary action to resolve any unsafe conditions.
Participate in required safety and quality training and other related activities.
Maintain good housekeeping in laboratory and working areas.

BASIC QUALIFICATIONS
Education/ AA in life science area with 1-2 years experience working in a similar environment or high school

Experience:
Diploma with 1-3 years experience working in a similar environment

Essential and Critical Skills:

Safe chemical handling methods
Communication skills, oral and written
Computer skills
Mechanical skills
Troubleshooting skills
Interpersonal skills
Organizational skills

BEOCS

Date Added: 10-15-2021

Manufacturing Operator 1 - Lenexa

15364

Lenexa, Arkansas

Manufacturing

BEPC Inc is looking for a Manufacturing Operator to join our fast growing team of consultants in the Lenexa, Kansas area!

Contract W2 Period: 6 months with possibility of extension

Pay/Benefits: $17.50 - 19.25/hour

40 hours per week / Mon-Fri 7am - 7:30pm or / Overtime will be paid at time and a half

Job Description:

End Date: 6 Months from start - Temp to perm for the right candidate
Training Hours: MUST BE ABLE TO TRAIN, MONDAY THRI FRIDAY 7AM-4PM for the first few weeks before switching to the 12 hour day shift. Accommodations in special circumstances will be considered.
Hours: 7:00 am - 7:30 pm day shift | 7:00 pm - 7:30am night shift(12 Hours/shift 4 Shifts one week, 3 the following week, totaling 84 hours every two weeks.

PAY: DAY SHIFT -$17.50/hr | NIGHT SHIFT - $19.25

Description:
Performs production procedures in accordance with Standard Operating Procedures (SOP), resulting in quality product.
Formulation Tasks:

Gather chemicals from different storage locations (i.e. room temperature, coolers and freezers);
use designated weights from 1 gm to 250 kg to verify scales; scoop and dump chemicals into containers up to 1,000 kg;
Place finished containers on a scale to verify gross weights;
Use a computer to capture production information;
Approve related reports and complete related documentation.
Blending and Milling Tasks:
Check rooms and equipment for cleanliness and damage prior to use;
Locate formulated chemicals for charging into blenders;
Setup and operate blenders in accordance with required specifications;
Setup and operate pin mill system in accordance with required specifications;
Setup and operate nitrogen conveying system; setup and operate clean-in-place (CIP) systems;
Control and monitor processes with an operator interface terminal (OIT);
Use a computer to capture production information; approve related reports and complete related documentation.

Packaging Tasks:

Use designated weights from 1 gm to 25 kg to verify scales are in specification;
Confirm material and supplies are staged; set up and operate automated packaging equipment within specified tolerances;
Fill powder into final containers up to 100 kg in weight;
Perform label reconciliation to ensure proper package labeling; move pallets of product to finished goods storage;
Approve related reports and complete related documentation.
Must be able to properly gown and comply with all cGMP and PPE guidelines
Set-up equipment ensuring operations are consistent with current operating procedures. Equipment components can weigh up to 50 kg and have critical tolerance requirements.
Report equipment failures and work with repair personnel to correct problems
Performs procedures resulting in the cleaning of manufacturing equipment and facilities.
Continually increases proficiency and understanding of manufacturing processes and systems.
Able to Read and Understand all written procedures as outlined in SOPs
Work Instructions and Master Batch Records (MBR).
Completes all documentation in accordance with current Good Manufacturing Practices (cGMP) and SOP.
Perform operations in compliance with rules and in a safe, orderly manner.
Participates in training programs as directed by the Department Supervisor. This may include monthly safety meetings, internal safety audits of operations, respirator training, and skill-based pay.
Follow production procedures and safety policies at all time.
Maintain good housekeeping in working areas.
Reports any unsafe working conditions or safety concerns through the corporate Medgate system.
Reports any property damage to the shift supervisor immediately
Takes part in and contributes to a safe working environment by following corporate and departmental safety regulations.
Use, clean, and store all personal protective gear appropriately
Makes recommendations for continuous process improvements in the manufacturing area.
Actively participates in Quality systems practices

Requirements

Education

High school diploma or equivalent with good math and reading skills.Experience
Experience in a manufacturing environment preferably with cGMP or regulatory compliance practices.
Demonstrated mechanical aptitude including previous maintenance experience with process equipment or mechanical systems.
Dry product processing and packaging experience.

Knowledge and Skills

Ability to read and follow written and verbal instructions.
Ability to perform basic metric and other mathematical calculations.
Ability to work independently and as part of a team.

Soft Skills

Works as a productive member of a team
Ability to effectively communicate with others.
Basic mechanical aptitude

Basic problem solving skills Required

Must be able to lift 5 pounds for a six hour period, or as required. Occasionally required to lift up to 50 pounds.
Must be able to maneuver and position mechanical components up to 50 kg.
Must be able to stand for long periods of time
Must be able to work within a controlled space without excessive perspiration

BEOCS

Date Added: 10-15-2021

Chemical Manufacturing Operations Technician

15361

Temecula, California

Other Area(s)

BEPC INC IS LOOKING FOR A CHEMICAL MANUFACTURING OPERATIONS TECHNICIAN TO JOIN OUR TEAM IN TEMECULA CA!

W2 CONTRACT: 1 YEAR WITH EXTENSION OR PERMANENCY POSSIBILITIES

PAY: $20.00/HR +MEDICAL DENTAL, VISION, LIFE INSURANCE.

Shift breakdown: 5:00 AM to 1:30 PM (Day), 1:00 PM to 9:30 PM (Swing), and 9:00 PM to 5:30 AM (Nights).

Candidate for this position must be able and willing to perform a variety of tasks in several different work functions and must demonstrate a mechanical aptitude.
Under general supervision, may be involved with the assembly, disassembly, testing and processing, packaging, consolidation, storage, inspection, labeling and shipping of chemical materials and hazardous waste.
Technician may also be involved with loading/unloading trucks and handling glassware.
Personnel in this position must possess sound interpersonal and communication skills as well as situational judgment and thought process to work effectively in a strong team-oriented environment.
In addition, the position requires basic understanding of the chemical properties being packaged as well as measures used to prevent exposure, contamination, or release to ensure a safe work environment. A focus on quality and attention-to-detail is a strong must.
Qualifications:
High school diploma or equivalent.
General industry experience preferably in a manufacturing environment.
Ability to read and understand Material Safety Data Sheets and technical drawings.
Ability to wear full face air-purifying respirator and other PPE.
Ability to lift 50 pounds and perform other physical tasks required by the job.
Must possess a strong mechanical background.
Must be willing to work night shifts.

KEY DUTIES:

Acid wash Teflon and stainless steel valves.
Acid wash of stainless steel vessels.
Disassemble, inspect, re-assemble and helium leak check of stainless steel container vessels and valves. Wash, dry and inspect quartz and borosilicate glassware.
Work in cleanroom and maintain integrity and housekeeping of cleanroom.
Utilize a computer to input and retrieve data.
Apply PVC coating to quartz and borosilicate glassware.
Perform quality inspections.
Package chemicals into quartz or stainless steel vessels.
Operate a forklift and unload trucks.
General Housekeeping duties.
Assist with inorganic and organic chemical consolidation.
Decontaminate certain stainless steel and quartz vessels and complete any required documentation.
Consolidation of hazardous waste.
Make computer entries to document all stages of customer returned items.
Understand and have knowledge of inventory control and cycle counting.
Ability to modify and repair both Pyrex and Quartz glassware.
Participate in Staple Ops Dent Collection and Review process.
Must be able to read and write fluently in English, understand written and verbal instructions and work well in a team environment.
Candidate will frequently lift / carry 25-35 lbs; occasionally lift / carry 36-50 lbs.
Candidate will be required to work with solvents of various types and may need to wear a respirator (infrequently if at all).

BEOCS

Date Added: 10-15-2021

Quality Control Core 3

15350

Spring, Texas

Other Area(s)

Clinical Trial & Data Management Expert 5

15344

Rockland, Massachusetts

Other Area(s)

Site Oversight & Delivery Activities:

Establish and manage site relationships, including but not limited to:
Act as liaison between the company and investigational sites, building investigator and site staff awareness on compounds
Develop and implement a plan, in collaboration with global and local teams, to raise the profile of the company and its global clinical development projects with current and potential investigators
Independently perform activities associated with the evaluation of investigational sites to build company network
Proactively work with Medical/Patient/Industry Associations to build company network and to promote company clinical trials
Develop knowledge of site capabilities and past performance to assess their potential as participating sites in clinical trials
Ensure regular communication with local organization to align interactions with KTLs and other relevant local/regional stakeholders
Oversee site-level study start-up, conduct, and close-out activities outsourced to CRO(s) for global programs across Therapeutic Areas
Support Site Agreement negotiations, including stand-alone and Master Site Agreements
Identify trends, issues and risks across sites, and work with external vendors and internal Trial Team to resolve/mitigate those
Collaborate with external vendors and internal Trial Team, to ensure that sites are activated in a timely manner and according to agreed timelines
Collaborate with external vendors and internal Trial Team, to ensure that sites deliver on expected recruitment targets, including identifying reasons for non-recruitment, and identification of non-performing sites that require actions
Ensure ICH/GCP/local regulatory requirements are observed
Senior Manager, Clinical Site Lead (CSL)
Provide documented sponsor site oversight at country level for outsourced trials in country under remit as required by regulation
Utilize site performance and quality data to optimize prioritization of oversight actions

Associate Director, Senior Clinical Site Lead:

Drive documented sponsor site oversight at country level for outsourced trials in country under remit as required by regulation
Utilize advanced analytics to optimize prioritization of oversight activities

In addition, employee may be assigned one or more added value roles:

Therapeutic Area Expert Assignment:

SME with focus to increase disease knowledge within the team by sharing materials (training/articles/abstracts) and/or arranging training sessions

Country Start-up Specialist Assignment:

Ensure that clinical sites in country(ies) of responsibility are activated within agreed timeframe and company agreed cycle times
Work closely with respective Clinical Site Leads to support them in issue resolution for site activation
Collaborate with external vendors to identify process(es) requiring improvement at the country level, build action plans to strengthen/improve those and track impact of actions
Support OSM model by acting as a local SME

Clinical Trial Delivery Lead Assignment:

Identify trends and issues within/across assigned trial(s) which may impact key deliverables (e.g. timelines/quality/costs) and implement action plans to either resolve and/or mitigate those
Advise the Trial Team on trends/issues and facilitate solutions, working closely with the CTL to ensure Corrective & Preventive Actions are defined and implemented.
Raise awareness of such trends/issues with Clinical Site Leads and other internal and external stakeholders as appropriate, including ICSO/CTE Leadership
Develop, implement and follow up on strategic action plans to drive improvements in site activation and/or enrolment, in collaboration with the CTL, CRO(s) and working closely with the respective Clinical Site Leads
Participate in Investigator/Study Coordinator Meetings and promote information sharing with the Clinical Site Leads as needed

Director, Principal Clinical Site Lead (additional responsibilities)

Manage company/department improvement initiatives as leadership role, with strategic impact and delivery accountability.
Take the lead and be the business process owner of the expert area, responsible for:

to define process goals
to design and document business requirements
to ensure harmonization and standardization of the process
to act as interface between functional managers and process team
to ensure implementation of optimization measures
for process monitoring/controlling, analysis and continuous improvement

Has good organizational understanding, relevant product, Clinical research landscape knowledge and ability to leverage this expertise to achieve objectives
Interprets and anticipates internal and external business challenges and recommends best practices to drive process improvements
Is recognized as an expert within ICSO and beyond; with peers within the same technical area in the business; as well as other key business functions
Serves as best practice resource within ICSO; may also act as a technical expert on cross-functional teams or projects
Handles sensitive issues and guides, influences and convinces colleagues in other teams/functions as well as external partners
Impacts through successful execution of projects within ICSO/CTE
Oversee external providers as applicable

Cooperation Internally

• CTE Functions
• Early & Late Stage Dev Operations
• Development Unit Clinical Leads
• (Global) Medical Affairs
• (Global) Regulatory Affairs
• SBDO China & Japan
• R&D Quality
• Other functions as needed

Cooperation Externally

• Clinical Research trial sites (Institutions/Investigators)
• Ethics Committees/ Regulatory Authorities (e.g., ECs/IRBs); if applicable
• Hospital administration
• Pharma Industry working groups
• Vendors (CRO)
• Patient Associations

Education:

Requires graduate background (Medical or Life Sciences degree) in a clinical research related discipline or equivalent

Work Experience:

Detailed understanding of all aspects of clinical protocol design and implementation, clinical site monitoring as well as overall global drug development
Expert knowledge of clinical development (principles and concepts as well as regulatory environment e.g. ICH GCP and applicable regional/local regulations)
Oncology and/or Neurology and/or Immunology TA experience desired

Senior Manager, Clinical Site Lead (CSL)

Substantial (8+ years) experience in clinical operations in a CRO, pharma or biotech company including site management/oversight, and site-level clinical study conduct

Associate Director, Senior Clinical Site Lead

Extensive (10+ years) experience in clinical operations in a CRO, pharma or biotech company including site management/oversight, and site-level clinical study conduct

Director, Principal Clinical Site Lead

Extensive (15+ years) experience in clinical operations in a CRO, pharma or biotech company including site management/oversight, and site-level clinical study conduct

Job specific Competencies & Skills

Strong communication skills (verbal, written and listening) in both native language and English
Aptitude to interpret and to integrate site performance data in prioritization of oversight activities
Ensuring compliance with applicable T&E Policy requirements
Role requires domestic and international travel up to 50% of time

Senior Manager, Clinical Site Lead (CSL)

Ability to work independently on assigned tasks or projects of increasing complexity
Capability to perform self-training incl. on therapeutic area, and synthesize the key take-away points for studies under remit
Normally receives no instruction on routine work and only general instruction on new assignments
Sound negotiation skills and adapting to a variety of parties
Record of vendor interactions
Sound critical thinking skills and ability to understand complex patient histories, medical terminology and specific therapeutic area treatment landscapes
Detail-oriented, organized and committed to quality and consistency
Results driven and capable of managing competing high-priority assignments
Proven track record of achieving deliverables within specified timelines
Ability to work in a dynamic environment with a high degree of flexibility
Ability to communicate effectively with Key Opinion Leaders, site staff, and internal team members
Experience and proven proficiency in CTMS and eTMF systems preferred

Associate Director, Senior Clinical Site Lead / Director, Principal Clinical Site Lead

Ability to work independently on assigned tasks or projects of increasing complexity and/or sensitivity
Capability to perform self-training and - if assigned as an SME (TA Expert, Country Start-Up Specialist, Trial Clinical Site Lead) - able to lead, coach and train other team members
Clearly conveys and receives information and ideas through a variety of media to individuals or groups, both internally and externally in a manner that engages the listener, helps them understand and retain the message, and invites response and feedback.
Uses appropriate interpersonal styles and techniques to reduce tension and/or conflict between two or more people; able to size up situations quickly; able to identify common interests; facilitates resolution.
Acts without being asked or required to; achieves goals beyond job requirements; being proactive; taking prompt action to accomplish objectives
Effectively exploring alternatives and positions to reach agreements and solutions that gain the support and acceptance of all parties.
Record of successful vendor interactions
Record of risk taking
Ability to build constructive working relationships with KOLs and clinical site personnel, other departments, and stakeholders

BEOCS

Date Added: 10-15-2021

Web & App Design Expert 1

15343

St. Louis, Missouri

Other Area(s)

Account Management Expert 2

15342

St. Louis, Missouri

Management

Packaging Operator 1

15324

Sheboygan Falls, Wisconsin

Manufacturing

BEPC INC. IS LOOKING FOR A PACKAGING OPERATOR 1 IN SHEBOYGAN FALLS WI!

W2 CONTRACT: 1 YEAR WITH EXTENSION OR PERMANENCY POSSIBILITIES

HOURS: 7am-3:30pm, Monday-Friday

PAY:$16.50+ MEDICAL, DENTAL, VISION AND LIFE INSURANCE.

Job description:

To stage, fill (manually or semi-automatically), cap, label and over pack liquid products per approved packaging specifications while utilizing all required safety equipment.

• Complete appropriate packaging documentation per ISO procedures and deliver products to inventory

• Fill, cap and label chemical products

• Follow all quality and safety procedures

• Support quality systems

• Ability to train others and work in a team setting

Physical Attributes:

• Wearing of appropriate protective gear, (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protection equipment "PPE" to protect themselves from toxic or corrosive chemicals in the forms of liquids, solids, vapors or airborne particles.

• The work area may occasionally be wet, humid abnormally hot or cold

• Siting, standing, walking, reaching above the shoulder, stooping, kneeling, twisting, crouching or crawling for long periods of time

• Talking, hearing, tasting and smelling

• Occasionally lift and/or move up to 50 pounds unassisted and ability to push and pull heavy materials to complete assignment; May lift more poundage with assistance.

• Utilize vision, distance vision, color vision, peripheral vision, depth vision, and the ability to adjust focus

• Uses phones, computers, computer monitors and office/manufacturing equipment

• Typing at a computer keyboard and ability to read CRTs/computer monitors

Minimum Qualifications:

• High School Diploma, GED or HSED required

Preferred Qualifications:

• Chemistry or 6 months chemistry related work experience

• Read instructions and understand oral and written instructions

• Basic math skills including the metric system

• Learn SOP's/UOP's, cleaning protocols, work and conduct rules

• Learn to use safety equipment. Learn to use semi-automated equipment

• Eye-hand coordination. Small/large tool dexterity

• Legible handwriting, teamwork, communication skills

• Problem solving

• Good time management and organizational skills

• Ability to operate a forklift

Date Added: 10-15-2021

Technical Sales Support Expert 1

15320

Burlington, Massachusetts

Technical

BEPC inc is looking for a TECHNICAL SALES SUPPORT EXPERT in Burlington MA.

W2 contract for: 1 year with extension or permanency possibilities.

Pay: $ 28.25/Hr. + Medical/ dental/ Vision/ Life insurance.

Hours: 40 Hrs /Week

JOB DESCRIPTION:

Will be part of the AI-enabled Drug Discovery Software, with a focus on sales and work closely with the Business Lead. A newly formed team responsible for development and commercialization of an exciting and transformational AI-enabled software solutions for small molecule drug discovery.

• Work as an expert superuser of our AI/Cheminformatics software product to independently provide highly technical presentations and software demonstrations
• Work closely with the business lead to develop and implement an effective cheminformatics marketing strategy
• Drive pre-sales activities including developing and planning solution presentations, demonstrating conceptual & proposed solutions, providing technical/product guidance etc.
• Pursue and develop sales opportunities with sales teams
• Identify new sales opportunities by researching and identifying potential accounts and leveraging networking opportunities (i.e. conferences, industry forums, etc.)
• Work closely with Sales teams to deliver and manage quotes, CDAs, negotiate contracts for sales of software license to customers
• Provide advanced training and follow-up with excellent client support during onboarding and throughout lifetime of contract
• Support training for internal stake holders in general sales, technical support, and sales support.
• Work cross-functionally with Product Engineers to address any technical questions and represent the product expertise of Cheminformatics software product
• Provide feedback & make recommendations to product, engineering, and marketing teams on market needs
• Network with Key Opinion Leaders in the Industry to gain insights into current trends and build trust around our technology

Physical Attributes
• Travel may be approximately 20-30% domestically and/or internationally

Minimum Qualifications:
• Master's Degree in Chemistry, Cheminformatics, or related technical discipline
• 2+ years of experience using Cheminformatics software
• 2+ years of experience in a technical sales or customer facing role

Preferred Qualifications:
• Ph.D. and MBA a plus
• Experience in a sales of cheminformatics tools, or any chemistry software solution
• Self-motivated and energetic

BEOCS

Date Added: 10-15-2021

Warehouse Coordinator

15307

Plano, Texas

Manufacturing

Test Technician Level 4

15306

Phoenix, Arizona

Technical

Executive Support Consultant

15305

Newark, New Jersey

Professional

BEPC is seeking 2 skilled Executive Support Consultants to join our fast-growing team of consultants in Newark, NJ!

W2 Contract Period: 9 months with possible opportunities for extensions based on business needs and performance!

Pay Rate: $41.63/HR plus we offer Medical, Dental, Vision and Life Insurance benefits!

A flexible multitasker who takes initiative, thrives in a fast- paced environment, and can working independently. Reporting across the Content organizations senior leaders, the ideal candidate will be able to quickly shift priorities as different needs arise.

You are comfortable operating in an agile environment, and possess solid experience successfully navigating the complexities of a large organization. You are a strong team player with exceptional attention to detail.

ABOUT THE ROLE:

Proactively manages Executives’ calendars, including scheduling large and/or complex meetings with external parties (key customers, such as top agents, production companies, and their coordinators/assistants), teams or high-level executives who may also work in different time zones
Work closely with fellow coordinators/executive assistants to accommodate more complex meetings involving senior management
Providing relationship management support, which may include follow-up requests/calls, data entry, and more
Identifying administrative needs for the organization and initiating projects to support those needs
Perform other administrative support duties, as appropriate (e.g., Visitor registration, parking, etc.)

QUALIFICATIONS:

Excellent interpersonal skills and professionalism are crucial
Familiarity with Outlook and the Microsoft Suite (Word and Excel in particular)
Strong verbal and communications skills
Strong organizational skills
Strong prioritization skills and ability to multi-task
Ability to work in a fast paced and evolving environment

BEPRO

Date Added: 10-15-2021

Laboratory Operations Core 2

15304

Rocklin, California

Manufacturing

BEPC is looking for a talented Lab Technician to come join our fast-growing team in Rocklin, CA!

Contract W2 period: 1 year contract with possibilities for extensions

Shift: M - F, 7am - 4pm

?Pay Rate: $18.30/hr

Job Description:
The Lab Tech participates in entry-level lab production duties, such as filling antibodies, labeling, packaging, shipping and other duties as assigned

Essential Duties and Responsibilities:

Filling Antibodies
Maintains the filling area stock and cleanliness as needed for continuous use.
Practices sterile techniques during the use of equipment specific to filling tasks.
Utilizes micropipettes, repeater pipettes, and pump systems to extract and dispense solutions into appropriate container, according to standard operating procedures.
Labeling
Assembles and washes dispensers used for product filling.
Prints and applies product labels based on a production plan.
Packaging
Packages products using standardized techniques and practices.
Stocks area inventories as necessary.
Shipping
Processes and packages orders internally using associated computer programs, equipment, and documentation.
Pulls products for shipment based on picking sheets.
Facilitates and maintains communication with production department and the customer service department to ensure that all orders are shipped as needed.
Packs product for shipping based on company standards.
Stocks products as necessary.
Maintains organization and cleanliness of the shipping and receiving area.
Signs for shipments to the company
Interacts with the customer service staff to complete special order requirements.

Requirements:

High school diploma or equivalent education required.
Minimum of 1 year production experience required.
Experience working in an FDA or other regulated industry preferred.
Lean manufacturing experience preferred.
Shipping experience preferred.
GMP (good manufacturing practices) or GDP (good distribution practices) expert preferred
Lab experience with pipette usage preferred
SAP system experience preferred
Able to work flexible hours

Skills:

Writes clearly and informatively.
Speaks clearly and persuasively in positive or negative situations; listens and gets clarification.
Able to add, subtract, multiply, and divide three digit numbers.
Able to read and comprehend simple instructions, short correspondence and e-mails.
Able to write simple correspondence and e-mails.
Able to effectively present information and respond to questions in one-on-one and small group situations of employees of the organization.
Experience with emails and calendaring required. Prefer experience with Microsoft Office Suite (Word, Excel, PowerPoint).
Multi-tasking
Attention to detail
Quick learning

Physical Requirements/Work Environment:

Must be able to lift up to a maximum of 50 lbs. on occasion without assistance.
Be able to handle repetitive type work

BEOCS

Date Added: 10-15-2021

Material Handler II

15303

Tualatin, Oregon

Manufacturing

US - Clinical Trial & Data Management Expert 2

15302

Rockland, Massachusetts

Other Area(s)

W2 contract period 11months

100% Remote

Pay rate: $43.40

Description

Accountable for day-to-day activities of all aspects for the management of local and/or regional company sponsored studies, including study plans, timelines, resources, allocation and management of product (re-) supply, problem identification and resolution, status reports and budget to ensure timely delivery of completed study reports to the project teams.
Accountable for the oversight of Investigator Sponsored Studies or Collaborative Research Studies granted by Merck, including the operational assessment of investigator-sponsor, tracking of performance and monitor budgets according to approved plans managing product supply (if applicable), coordinating internal review of final report.
Manage External providers and/or independent consultants including CROs, Full Service Provider teams, clinicians, etc.) when required by the project including and not limited to, oversight of the activities and coordination of project specific training, etc.…

Duties

Develop and monitor study budget and timelines.
Monitor work to ensure quality.
Ensures that trial status is accurate and up-to-date in Clinical Trial Management System.
Contribute to the planning and set-up of a study and provide planning parameters, Support early access programs on the country level of the services you require.
Provide product expertise and/or oversight at the country level to external consultants and/or flexible staff working on company sponsored clinical studies.
May be assigned one or more SME roles within ICSO or CTE functions (eg. Lead at the Country level early access programs in collaboration with the Program Clinical Delivery Lead)

Requirements:

Bachelor of science
4-5 years of experience

Additional experience required

5 years of direct trial management experience (pharma or CRO).
Work independently, be a quick learning, be able to navigate multiple complex reporting systems, able to train-grasp and understand multiple SOPs and the interconnectivity between functions/department, be good at multi-tasking and effective prioritization or work, have a fundamental understanding in soft skills (e.g., conflict management, successful negotiations, communication skills)

BEOCS

Date Added: 10-15-2021

US - Customer Care - Call Center Expert 2

15301

Rockland, Massachusetts

Other Area(s)

Job Summary:
The Patient Support Navigator (PSN) interacts directly with customers to address their concerns, such as requests for product or device related information, program fulfillment materials, and coordination of home nurse training requests. The PSN also provides reimbursement and nurse triage support. The main goal of the PSN is to achieve a high-level of customer satisfaction and case resolution.
Responsibilities:
• Answers inbound calls and documents information accurately in the program database.
• Manages customer information with the strictest of confidence, in a professional, empathetic and customer centric way.
• Interacts directly with patients, caregivers, and healthcare professionals.
• Calls must be answered promptly, professionally, and compassionately with the result of meeting the customer’s needs.
• Ability to problem solve and determine appropriate actions for issue resolution. Actions may include contacting pharmacies to clarify prescription information, insurance companies to confirm benefits, and physician’s offices in a collaborative fashion to resolve patient issues.
• Manage replacement requests of our products or devices for patients. Exercise good judgment on when to expedite delivery based on needs or available options.
• Provide patients, caregivers, physician/nurses or other healthcare professionals with approved product information.
• Update Managers/Supervisors with feedback from customers to improve services or provide recognition of team members.
Professional Qualities:
• Experience in the healthcare field (e.g. medical, pharmacy, bio-tech, insurance or reimbursement) with customer care experience preferably with patient interaction or educational support.
• Experience with handling of inbound and outbound phone calls, database enrollment and operational activities.
• Effective listening, written and verbal communication skills.
• Must be comfortable using multiple communication methods, including phones, internet, email, faxes or text messaging.
• Effective interpersonal skills to interact with a diverse group of professionals and personalities in a team environment
• Must be flexible with the ability to multi-task to ensure accurate data entry
• Strong computer skills (customer contact databases, salesforce.com, Microsoft Office applications (Windows, Word, and Excel) required.
• Strong data entry/typing skills.
• College degree or equivalent
• Bilingual a plus
• Must be flexible to work hourly shifts, weekends and certain holidays, or holiday weekends. Overtime may be available.

Date Added: 10-15-2021

Versum - Analytical Technician I

15297

Tamaqua, Pennsylvania

Other Area(s)

General Research & (Clinical) Development Expert 1

15296

Carlsbad , California

Professional

BEPC Inc is looking for a General Research & (Clinical) Development Expert 1 in Carlsbad, CA!
Contract W2 Period: 3 Months contract with possibilities for extensions
Pay & Benefits: $37.75/hr. +Medical, Dental, Vision and Life Insurance

Description:

On- Site or Remote: Remote- 90% remote/ 10% on-site (report to office to get documents)
Hours: standard hours 9-5pm

Skills:

Must have knowledge on production facility language/ experience to know how to investigate it
Interacting skills, writing
Quality Systems "nice to have, but not a requirement"

Your Role:

Determines the root cause and corrective action for deviations identified in various production processes.
Ensures that investigations identify true root cause and appropriate corrective actions in order to prevent recurrence.
In this role you will provide technical expertise within the context of defining the problem statement, assessing the impact, identifying root cause, and determining corrective actions, communicate cross-functionally effectively and professionally to lead investigative discussions, work independently and as part of a team to manage multiple projects simultaneously.
You will need to have the ability to distill complex thoughts and issues so that an educated, but unfamiliar reader can understand and make decisions based on the written investigation report, be organized and detail oriented as well as an active listener and communicator.

Basic Qualifications:

Bachelor’s degree in life sciences or related scientific discipline

2+ years’ experience in regulated environment

Preferred Qualifications:

Experience with CAPA’s highly preferred
Experience with deviation tracking system (e.g. Trackwise) and conducting investigations highly preferred
Thorough understanding of the biopharmaceutical manufacturing process, current Good Manufacturing Practices highly preferred
Experience working with quality tools (Fishbone Diagrams, 5 Whys, etc.)
Good analysis, troubleshooting, investigation and communication skills, both written and verbal

BEOCS

Date Added: 10-15-2021

Operator I

15295

Temecula, California

Manufacturing

Mon – Fri (5am/6am – 1:30pm/2:30pm)
OT may be required

This position is responsible for the production of high-quality medical devices within a manufacturing cell. Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies. Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed.

Duties & Responsibilities:

Ensure that relevant job documentation for cell operations and functions is accurate and up to date
Be able to clearly communicate ideas, problems, and solutions to all levels of manufacturing management in both written and oral for
Maintain a positive attitude when interacting with internal customers and external customers such as tours
Follow safety guidelines and utilize appropriate safety devices when performing all operations
Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics
Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products
Demonstrates a basis understanding of Lean Manufacturing
Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations
Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements

Requirements:

Verbal and Written Communication
Understanding of and ability to utilize electronic data collection systems and computer software packages
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance
Routinely handle and maneuver small components and parts
Ability to make critical decisions and judgments with minimal supervision

Education:

High school degree or equivalent preferred

BEOCS

Date Added: 10-15-2021

Biology Expert 1

15294

Rockville, Maryland

Other Area(s)

BEPC INC IS LOOKING FOR A BIOLOGY EXPERT IN ROCKVILLE MARYLAND!

HOURS: 8-12 week training that is 1st shift (M-F; 8am -5pm)
After training, converts to 2pm- 10:30pm (10% increase in pay)

PAY:$25.75/hr +MEDICAL/DENTAL/VISION/LIFE INSURANCE

W2 CONTRACT:10 months w/extension or permanency possibilities.

REQUIREMENTS

· PCR, or qPCR experience.

· BS education

Activities include:

· All aspects of research, technology development, product development, solution development and testing.

· Initiates, directs and executes scientific research and/or development related to Biology, Biochemistry and Virology.

· Investigates feasibility applying a wide variety of scientific principles and concepts to inventions, products, and problems.

IMPACT:

· Impacts the results of own team with own contributions.

COMPLEXITY:

· Performs routine assignments using existing procedures OR works autonomously within established procedures and practices that require knowledge of concepts and procedures within a job discipline OR specialized technical expertise within an analytical/scientific method or operational process.

ACCOUNTABILITY/ INDEPENDENCE:

· Accountable for the quality of own work.

· Receives instruction, guidance and direction from more senior level roles.

EXPERIENCE:

· Typically graduate background with little professional experience.

· Non-graduate jobholders require a substantial amount of professional experience and additional qualifications that also provides exposure to fundamental theories, principles and concepts.

· Typically reports to a Manager role, Project Manager role for a defined period of time based on organizational set-up (there is not necessarily a difference in role level between a manager and its direct reports - same level or lower level reporting is possible, provided job scope and responsibilities are clearly distinct); typically no direct reports.

EDUCATION:

· BS or AS degree and 1-2 yrs experience

· or HS Diploma/equivalent and 5+ yrs experience

Date Added: 10-15-2021

Test Technician Level 2

15291

Phoenix, Arizona

Other Area(s)

Technical Change Management Documentation Specialist

15288

Oceanside, California

Biotech/R&D/Science

BEPC has an open position for a Technical Documentation Specialist in Oceanside, CA!

Contract W2 Period: 9 month contract with possibilities for extensions
Pay & Benefits: $51/hr. + Medical, Dental, Vision and Life Insurance

Coordinate and document technical changes for Technical Transfer projects in Trackwise.
Coordinate and execute document changes for Technical Transfer projects.
Coordinate, execute and document Design Qualification for Technical Transfer projects.
Draft change records and document deliverables in Trackwise
Execute document changes in Syncade and Condor
Manage, generate, modify, and support GMP documentation and drawing changes.
Update/report completion in project schedule.
Export data and create metrics/charts to report status
Ensure deliverables are completed and documented in time to meet project milestones
Review all project GMP documentation.
Assist in the Science & Engineering change control process in accordance with SPO02411, GSP047, GSP026 and new documentation processes as they are developed.
Assist with generation of project workflows.
Assist with generation of project work instructions.
Assist with generation of project schedule templates.
Lead project meetings and generate meeting agendas and minutes.
Assist with generation of Science & Engineering business processes.
Translating Ideas into Specifications, Work Instructions, and Standard Operating Procedures
Skills
Strong Knowledge of Good Manufacturing Practices
Strong Technical Writing Skills
Troubleshooting & Problem-Solving
Gathering, Collating, Assimilating Information
Working with Teams to Complete Projects
Organizational & Analytical Abilities
Attention to Detail, Goal-Oriented Focus
Ability to Seek and Use Input from Target Audience
Education
BS degree with a minimum of 6 years experience. An advanced degree (MBA or MS) is a plus.

BEOCS

Date Added: 10-14-2021

Senior Principal Engineer IV

15287

South San Francisco, California

Engineering

Description:
Important: Genentech has mandated COVID-19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Genentech are required to comply with this requirement.

The process engineer will manage the development and transfer of manufacturing processes
for medical devices and drug device combination products at an external manufacturing site.
Job duties will include but are not limited to the following:
The candidate should be proficient in the following general areas –
• Medical device development per 21CFR820.30 and ISO 13485.
• Management of contract manufacturing organizations.
• Collaboration with internal and external suppliers at a detailed technical level with
design engineers, equipment, and production engineers.
• Review of technical reports including statistical analysis of data.
• Equipment procurement and qualification including GAMP5.
• Risk management per ISO 14971.
• Process validation
The candidate should have specific technical expertise in the following topics –
• Development of custom automation including process optimization.
• Development and procurement of packaging equipment for sterile barrier systems.
• Process FMEA and risk management.
• Clean room manufacturing operations.
• Semi-automated and automated vision system inspections (development and
validation).
• Familiarity with injection molding and micro molding.
Additionally, the candidate should have experience with the following –
• Internal quality assessments/audits, regulatory inspections, and notified body
interactions.
• Discrepancy and change management.
• Authoring documents to support device development: design verification
protocols/reports, d/pFMEAs, risk management plans, design transfer plans, and change
management plans.
The candidate should possess the following interpersonal skills –
• Proven track record of working effectively in a matrix organization with a highly crossfunctional (e.g., validation, quality, regulatory, and program management) and
collaborative environment.
• Excellent oral and written communication skills.
• Excellent leadership skills.
• Success in project planning, resource management, and liaising with engineering and
manufacturing resources, potentially in other countries.

Education
B.S, M.S, or advanced degree in engineering, with preference for mechanical or
chemical engineering, or the equivalent.
• At least 10+ years of experience in the industry and/or academia (including advanced
studies) after receiving their Bachelors degree.

BEOCS

Date Added: 10-14-2021

Organizational Change Manager II

15286

Oceanside, California

Biotech/R&D/Science

BEPC Inc is looking for an Organizational Change Manager II in Oceanside, CA!
Contract W2 Period: 1 year contract with possibilities for extensions
Pay & Benefits: $68.79/hr. +Medical, Dental, Vision and Life Insurance

*** This role is remote and does not need to be in Oceanside. ***

*** 20hr Shift (4hr/day) ***

Purpose:

Organizational Change Management Expert for the project ‘Global Release Execution System’; Global Quality in Pharma Technology (PT). The goal of the project is to Improve Efficiency and Compliance of Batch Release globally.
Provides Project Management expertise utilizing standard tools and consistent methodology

Job Description:

Organizational change management (OCM): Assess and manage stakeholders, develop and drive OCM activities.
Continuously assess sponsorship effectivity, OCM risk profile, and stakeholder communication clusters and initiate required activities for sustainable project success.
Support project management to successfully complete the project, report project status and progress to the program management and stakeholders.
Independently manage and track OCM-related project activities and dependencies to other projects.
Implement stakeholder trainings including respective GMP and regulatory compliance requirements.
Business analysis to identify and implement the ideal communication strategy based on cross-functional business requirements.
Applies a complete understanding of the project management process and methodology and delivers to all aspects of the project lifecycle for global and cross-functional projects/initiatives
Independently addresses a broad range of difficult problems while managing priorities and tasks across a project
Reviews and provides input on deliverables & recommendations
Demonstrates judgment in selecting methods, tools and techniques for obtaining solutions
Enables project culture that is value and quality focused
Takes ownership drives towards completion

Qualifications:

BA/BS degree with 7 years experience in healthcare/ biotech/ pharmaceutical industry a plus; Roche experience is a plus
Strong communication and OCM skills (PROSCI certification preferred)
PMP Certification preferred (PMI or similar); experienced in managing projects with an IT component
Strong analytical and problem solving skills
High quality orientation with attention to detail; drives for excellence and positive business outcomes
Excellent collaborator with proven ability to work well with others in a proactive, positive and constructive manner
Strong self-motivator who can manage multiple priorities
Knowledge of manufacturing, cGMP's and compliance
Demonstrated influencing and interpersonal skills with strong written and verbal communication skills; ability to communicate effectively with all levels of the organization

BEOCS

Date Added: 10-14-2021

Mechanical Engineering SME

15285

South San Francisco , California

Engineering

BEPC has South San Francisco, CA open position for Mechanical Engineering SME to join our fast-growing team of consultants!

Contract W2 Period: 8 months with possibilities for extension
Pay & Benefits: pay/hr + Medical, Dental, Vision & Life Insurance
Location: 1 DNA Way South San Francisco California, United States

Ref: 15285 - ROCGJP00013422

Description:

Support ongoing projects with mechanical SME services:
Provide technical mechanical SME support and accountability to Genentech SSF Design & Construction for all aspects of mechanical design review and construction support on assigned capital and expense projects at the SSF campus.
Support architectural, engineering and construction firms selected by Genentech for the design and construction of the projects as the Genentech owner representative.
Support design and planning of upgrades to critical and non-critical mechanical systems.
Ensure that project designs provide safe, efficient and reliable operations to Genentech.
Support the execution of a portfolio of projects with technical input and coordination in the mechanical discipline.
With minimum oversight, Vendor shall provide design guidance on HVAC, Plumbing, Piping and Fire Protection systems.
Attend key design meetings and provide design input and technical options analysis in accordance with Genentech global and site standards
Coordinate input to and influence key customers (R&D, Commercial, Pharmaceutical Technical Operations) and stakeholders (Site Operations, EH&S, Maintenance & Plant Engineering) on project designs.
Establish a working relationship with the lead engineers of the Genentech three Alliance Design Partners in addition to Site Operations, Environmental Health and Safety, Global Engineering and other stakeholders. As defined by project needs and with general guidance from the principal engineer, the mechanical SME shall work directly with all project stakeholders to develop strategies for upgrading deficient areas of the campus throughout the project portfolio.
Review and comment of engineering design documents prepared by Genentech’s engineering consultants with respect to HVAC, Plumbing and Fire Sprinkler systems and utilities.
Work with the architectural/mechanical engineering consultant and Genentech and the general contractor’s personnel, to review mechanical design, cost and scheduling documentation for the mechanical systems.
Work with Genentech BAS personnel to determine the temperature controls (BAS) requirements for the projects.
Work with the acoustical consultant to ensure that the HVAC and plumbing systems do not adversely impact the acoustical and vibration goals of the projects
Review and comment of cost estimating packages prepared by the architectural/mechanical engineering consultants and the General contractor.
Provide engineering support for Roche K18 energy analysis and NPV (Net Present Value) calculations purposes.
Perform site visits of the existing conditions to be acquainted with the existing HVAC, plumbing and fire sprinkler systems.
Participate and attend design, risk and review meetings as needed - attend weekly project meetings in SSF or via remote access.
Assist in guiding contractors and consultants on Genentech standards

Education

B.S or M.S. in Chemical, Electrical or Mechanical Engineering with 3-5 years experience or equivalent degree and relevant work experience/training.

BEOCS

Date Added: 10-14-2021

Research Associate II

15284

South San Francisco, California

Biotech/R&D/Science

BEPC Inc is looking for a Research Associate II in South San Francisco, CA!
Contract W2 Period: 11 months contract with possibilities for extensions
Pay & Benefits: $48.61/hr. +Medical, Dental, Vision and Life Insurance

PSR position in the T3 lab

This position is embedded within the Translational Tissue Technology (T3) core lab in the Pathology Department and focused on spatial transcriptomics (ST), spatial proteomics (SP) and higher order immunofluorescent multiplexing (4+markers), providing scientific expertise for tissue-based assays across the pathology core labs. The pathology T3 core is a state-of-the art lab equipped with automated platforms and various ST and PT technologies and focuses on the development of tissue based assays to support discovery research as well as early and late stage programs. Another focus of the T3 lab is the evaluation and implementation of new ST and PT technologies.

Duties

The main duties of the position include designing, planning and performing spatial transcriptomics, spatial proteomics or other higher order multiplexed IF assays for projects supporting different therapeutic areas.
The individual in this position will independently conduct studies from inception through assay development/experimentation to data interpretation, data analysis and reporting.
Candidates should enjoy associated challenges such as implementing new technologies and workflows as well as working across functional groups.
Other job relevant tasks include data acquisition (microscopy, scanning), image analysis, photographic documentation, recording, compilation, interpretation and presentation of results.

Skills

An addition to strong scientific credentials, candidates must have a record of productivity as well as relevant professional experience.
Candidates must enjoy handling multiple collaborative projects and working in a fast paced team-oriented environment.
Excellent communication, multitasking, organization, record keeping, problem-solving skills and the ability to work effectively in a team are therefore essential.
The position requires a high degree of independence and thorough understanding and proficient use of tissue based ST, PT and IHC techniques.
Candidates should have a desire to perform bench-work as well as data acquisition and data analysis.
In-depth knowledge and hands-on experience with microscopy and histology is a must. Experience with 10x Visium, Nanostring GeoMx or MERFISH is a plus.

BEOCS

Date Added: 10-14-2021

Planner / Scheduler II

15283

Oceanside, California

Professional

BEPC has an open position for a Planner/Scheduler II in Oceanside, CA!

Contract W2 Period: 1 year contract with possibilities for extensions
Pay & Benefits: $41.27/hr. + Medical, Dental Vision and Life Insurance

Duties

The Planner/Scheduler converts the master production schedule into a feasible detailed production schedule and materials for the OCN manufacturing site. As a key interface between Master Scheduling, Global Planning and site Operations and support teams, the Planner/ Scheduler is a team-player who collaborates with stakeholders to propose and make decisions to optimize the utilization of work center capacity and/or availability of raw materials while removing barriers to achieve the MPS. Using critical thinking and a continuous improvement mindset, the Planner/Scheduler takes a proactive approach to engage stakeholders in driving scenario analysis and resolution of problems.

Responsibilities include, but are not limited to, forecasting, scheduling, MRP review, automated system utilization, project management, continuous improvement, network collaboration, team facilitation, participation in operations meetings, driving departmental Class A activities and overall materials planning and production scheduling management for the Oceanside facility.

Skills

Perform all detailed scheduling, materials planning and forecasting activities to support the achievement of the Master Production Schedule and to build appropriate safety stock levels.
Manage all planned/process orders and purchase reqs/orders for specific MRP controllers or workcenters in a timely manner.
Independently resolve order management issues and escalate as required.
Working as a team, coordinate the production, materials and maintenance scheduling activities to drive alignment and resolve constraints.
Drive adherence to planning and scheduling timefences.
Company Confidential Coordinate planning and dispensing activities with multiple groups across sites.
Drive or participate in continuous improvement projects more than 15% of time to streamline and document scheduling processes, while eliminating waste in the order management process.
Conduct scenario planning, substantiate results and provide recommendation on best path forward.
Coordinate and drive projects to support Materials Management, FOS and Manufacturing.
Independently communicate and resolve materials and detailed scheduling issues.
Develop and track metrics for production and materials scheduling, forecasting, order management, schedule adherence, and inventory accuracy.
Conduct root cause analysis and implement issue resolution
Drive or support Class A re-certification efforts for the Site Scheduling department.
Support improvements to SAP APO, R/3, automation systems and other business system development.
Identify methods to leverage ERP systems and remove unnecessary spreadsheets and manual tools.
Ensure all processes are documented and provide cross-training and documentation for exception scenarios.
Actively participate as a vocal member in required meetings, including DCT, WST, wWST, LTT's and other required meetings.
Coordinate team to align, drive actions and resolve constraints to achieve the MPS.
All employees with jobs that require access to the Warehouse (TSA) Security Threat Assessment (STA must be able to pass the Transportation Security
Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt.

Education and Experience:

Bachelors degree or APICS certification
2-5 plus years of related planning or scheduling experience
Production Manufacturing/GMP experience required.

Knowledge/Skills/Competencies:

Experience with GMP procedures and concepts.
Knowledge of planning concepts such as APICS body of knowledge and world class manufacturing.
Experience in materials planning and production scheduling with a strong attention to detail while working in a fast paced and changing process manufacturing environment.
Ability to plan and schedule activities effectively while proactively identify potential issues to drive to resolution.
Fundamental knowledge of inventory, planning, and scheduling principles.
Strong ability to make independent decisions while taking into account varying perspectives in a fast paced and quickly changing environment.
Excellent written and verbal communication skills.
Strong facilitation and project management skills.
Demonstrated leadership qualities and ability to build relationships with teammates, internal and external customers. SAP APO / ERP experience preferred.
Advanced skills in MS Office (Excel/Word) preferred.
Ability to think outside of the box and have a continuous improvement mindset.

BEOCS

Date Added: 10-14-2021

Material Handler - Technician II

15281

Oceanside, California

Manufacturing

BEPC has an open position for a Material Handler-Technician in Oceanside, CA!!
Contract W2 Period: 5 month contract with possibilities for extensions
Pay & Benefits: $36/hr. + Medical, Dental, Vision and Life Insurance

Responsible for performing duties in the materials management function (pre-weigh, shipping, receiving and delivery of non-GMP materials).
Loads, unloads and/or conveys materials throughout the organization, performs a combination of tasks which may include shipping and/or receiving.
Materials maybe of a hazardous/ controlled nature requiring regulatory endorsements prior to handling.
Verifies quantity, weight, and conformance of materials; prepares records of materials shipped and boxes, and prepare parts and tooling for special shipment.
May develop reports or prepare metrics.
Responsible for performing duties within the Materials Operations.
Functions can include one or all of the following: Materials Operations and Logistics, Dispensary Operations and MRO Operations. Computer system/ERP knowledge, SAP and Delta V.
Move and storing cGMP and/ or non-cGMP materials.
Monitor critical equipment information.
Comply with safety requirements cGMP, SOP and manufacturing documentation.
Delivering and distributing dispensed material.
Comply with safety requirements cGMP, SOP and manufacturing documentation.
Delivering and distributing dispensed material.
May receive non-GMP materials and goods.
Account accurately for items in SAP.
Deliver accordingly to customers.
Manage GMP Inventory, control materials, issue to manufacturing.
Utilize SAP per WM Material Handler Security roles.
Safely Drive department MHE and perform basic preventive maintenance duties for material handling equipment (forklifts) including visual inspections and logbook documentation.
Handling of disinfectants, irritants, toxicants, and hazardous materials. For example; Vesphene, LpHse, Tetramethylammonium chloride (TMAC), Methotrexate (MTX), Sodium Phosphate Monobasic, Sodium Phosphate Dibasic, Potassium Hydroxide, Sodium Hydroxide, Phosphoric Acid, Hydrochloric Acid, Glacial Acetic Acid, Benzyl Alcohol, Ethanol, Isopropyl Alcohol
Ability to operate materials handling equipment; pallet jack, drum picker, fixed and mobile drum lifters, forklifts (mobile IBC lifter, “walkie-stackie”)
Distribution of dispensed materials (transferring IBCs, intermediate bulk containers, up to ~ 400 Kg gross weight)
Adhering to all cGMPs, Genentech policies, and SOPs.
Ability to use automated and paper based documentation systems.
Adhering to batch instructions (if necessary) and standard operating procedures.
Maintaining and accurately completely batch documentation.
Manage inventory of equipment parts and consumable materials in support of process development, maintenance, manufacturing, quality control and other related areas utilizing industry wide standard inventory control practices.
Perform parts staging for PM and other planned activities.
Maintain Kanbans for various customers.
Perform routine clerical duties including data entry, answering telephones and assisting over the counter customers.
All employees with jobs that require access to the Warehouse must be able to pass the
Transportation Security Administration (TSA) Security Threat Assessment (STA).
Follows established safety and environmental guidelines and procedures for all work performed.
Immediately reports safety and environmental incidents including injuries, illnesses, near misses,
and safety suggestions. Fosters a positive safety culture in which no one gets hurt.
Supplementary Responsibilities
Receive, inspect and document non-GMP standard stock items in accordance with department and SOPs.
Track post incoming general merchandise by entering information into an automated database.
Deliver packages and maintain accurate and complete documentation in delivery logbooks.
Collect non-Gmp materials for shipping and provide assistance with packaging, labeling and shipping documentation.
Perform basic preventive maintenance duties for material handling and delivery equipment and/or vehicles including visual inspections, logbook documentation and routine mechanical procedures.
Process capital asset materials by assigning and placing identification (asset) tags and update accounting/ finance records.
Dispense media and buffer components (raw materials) according to batch record instructions and standard operating procedures.
Responsible for accurately documenting batch records, following safety SOPs for hazardous materials handling.
Education and Experience
Associate Degree and 1-year experience or HS and 2-4 years’ experience
Minimum 3-5 year’s experience in warehouse or GMP regulated environment
Knowledge, Skills, and Abilities
Familiarity of computer-based systems.
Knowledge and experience with SAP is a huge plus.
Prior experience in a GMP, biotech, pharmaceutical, or chemical manufacturing environment.
Prior training in chemicals/powder handling/ dispensing, and good laboratory methods/ practices is preferred.
Valid driver’s license and good driving record.
Must be able to be Forklift Certified
Schedule could include one weekend day, evening or night hours, or full off-shift hours.
Expected to be on feet for 6-8 hours a day.
Climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility.
Lifting up to 50lbs may be required.
Environment may require gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn.
Exposure to level 1 chemicals.
May work in clean room environment with large mechanical equipment, piping, and pumps.
Will operate electric pallet truck and other material handling equipment.

BEOCS

Date Added: 10-14-2021

Materials Handler (Heavy) II - 2nd Shift

15280

Menlo Park, California

Manufacturing

Biomedical Technician

15277

Albuquerque, New Mexico

Manufacturing

BEPC is looking for a confident Biomedical Technician to come join our fast-growing team in Albuquerque, NM!

Contract W2 period: 24-month contract with possibilities for extensions

Pay: $26/hour

PURPOSE:
Responsible for supporting Albuquerque Sterilization Scientists with operations in the area of sterilization and new product integration activities.

EDUCATION/CERTIFICATION REQUIREMENTS:

Minimum of a Bachelor of Science in a Life Science or Chemical Engineering, required.

KEY SKILLS/KNOWLEDGE PREFERRED:

ISO Radiation Sterilization Standards.
Radiation dosimetry systems-- routing measurements and calibration.
Dose mapping of products in radiation fields.
Organizational / planning skills / Interpersonal / communication skills.
Thorough knowledge of and be able to apply/use the above skill set.
Able to deal with abstract and complex cause and effect relationships and make sound decisions, often with limited data, which impact products and facilities.
Basic word processing and spreadsheet skills using standard IBM software.

EXPERIENCE, PREFERRED

2 - 4 years experience and demonstrated proficiency in medical device sterilization or related industry.
Able to work effectively in a team environment, make effective management level presentations and write formal reports.
Training and experience in Good Manufacturing Practices

KEY JOB RESPONSIBILITIES:

Work on projects of various size and complexity, primarily on high impact complex projects.
Coordinate exposure of test samples to sterilization processes to support teams.
Support dose distribution studies strategies for complex product orientations.
Analyze dosimeter calibration data from internal irradiators and contractors.
Troubleshoot sterilization process deviations; develop short & long term solutions to prevent reoccurrence.
Follow all company safety policies and other safety precautions within the work area.
Promote safety to all associates that enter the work area.
Set standards for safe behavior. Recognize and reward safe behavior in others.
Enforce safety policies and procedures. Ensure that direct reports employ safe practices.
Other responsibilities may be assigned and not all responsibilities listed may be assigned.

WORK ENVIRONMENT:

Manufacturing environment
Participate in EMS management structure toward implementation and maintenance of EMS including continual improvement; pollution prevention; objectives and targets; and regulatory compliance.
Participate and support the ISO 14001 Certification and Regulatory Audit process.
Implement and follow all applicable EMS procedures.
Adhere to the sites EHS Code of Conduct.

PHYSICAL DEMANDS:

Office deskwork, requiring sitting, walking, using the phone and computer, may lift up to 30 lbs. occasionally.
Long walking, standing, bending, stooping and reaching.
Public speaking, visual assessment of facilities and products and ability to respond to visual and safety alarms.

TRAVEL REQUIREMENTS:

No travel may be required.

BEOCS

Date Added: 10-14-2021

Quality Assurance Core 2

15276

Rockville, Maryland

Manufacturing

Maintenance Mechanic

15275

Pomona, California

Technical

Assembler I

15274

Princeton, New Jersey

Manufacturing

Senior Materials Coordinator

15272

London, Ohio

Other Area(s)

Senior Materials Scheduler

15271

Urbana, Ohio

Other Area(s)

Electro/Mechanical Assembler 2

15270

Marlborough, Massachusetts

Other Area(s)

BEPC is ACTIVELY seeking a Mechanical Assembler to join our team of consultants in Marlborough, MA!

Contract W2 Period:3 month contract with possibilities for extensions

Pay & Benefits: $18.00/hr. + Medical, Dental, Vision and Life Insurance

Shift: M - F 7:00 AM - 3:30 PM

Summary of Duties and Responsibilities:

Responsible for building, testing and inspecting electro-mechanical assemblies per specification.
May involve system level assembly and sub-assembly test.
Assembles sub-assemblies and system level hardware
Performs in process sub-assembly testing of product being manufactured, when required
Completes Device History Record data
Performs assembly and test requirements for reconditioned hardware, when required
Perform packaging functions in Instruments Manufacturing, when required
Maintain compliance with Hologic policies (QSR, ISO, EH & S) · Proficiency with basic hand tools such as screwdrivers, wrenches, torque tools, terminal crimpers, and soldering irons.
Ability to follow written instructions such as assembly procedures, test procedures mechanical assembly drawings.
Experience with basic mechanical inspection equipment such as calipers and indicators.
Experience with basic electrical test equipment such as multimeters.
Supports the day-to-day operations of manufacturing and service support to forecast, and regulatory compliance and policies (QSR, ISO, EH & S)
Provides training as needed.
Participates in the reduction of risk and injury in the workplace by identifying risks and implementing controls to eliminate or minimize risk.
Supports internal departmental audits of manufacturing processes to ensure compliance with policies (QSR, ISO, EH & S).
Perform other duties as required.

Education:

High school diploma or equivalent experience/training.

BEOCS

Duties & Responsibilities: - Test, calibrates and repairs production machines and related subassemblies to written and/or oral specifications in a timely fashion . - Responsible for meeting or exceeding quality and efficiency standards. - Ensures quality and operation of work. - Reads and interprets schematics and blueprints required to ensure proper calibration of machines. - Timely and accurate testing and calibration of all electronic subassemblies and must clearly document results. - Ensure that design, implementation, test and maintenance methods/processes are developed as well as executed in a manner, which supports all Hologic's Quality Standards. - Perform other duties as required

BEPRO

Date Added: 10-14-2021

Operator I

15269

Liberty, South Carolina

Manufacturing

BEPC has a Liberty, SC area open position for Operator 1 to join our fast-growing team of consultants!

Contract W2 Period: 1 year with opportunity for extensions
Pay & Benefits: $13.60/hour + Medical, Dental, Vision & Life Insurance

Work Shift: 1^st Shift, 7am – 5:30pm

High school degree or GED.

This position is responsible for the production of high-quality medical devices within a manufacturing cell.

DETAILS:

This is a none exempt position.
Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.
Performs routine assignments according to specified and/or standardized procedures.
Work is closely and continually reviewed.
Ensure that relevant job documentation for cell operations and functions is accurate and up to date.
Be able to clearly communicate ideas, problems, and solutions to all levels of manufacturing management in both written and oral form.
Maintain a positive attitude when interacting with internal customers and external customers such as tours.
Follow safety guidelines and utilize appropriate safety devices when performing all operations.
Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.
Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Demonstrates a basis understanding of Lean Manufacturing. Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions
Understanding of and ability to utilize electronic data collection systems and computer software packages.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to handle and maneuver small components and parts.
Ability to make critical decisions and judgments with minimal supervision.
High school degree or equivalent preferred.

BEPRO

Date Added: 10-14-2021

Warehouse Coordinator

15268

Plano, Texas

Manufacturing

Engineer - Degreed II

15267

Los Angeles, California

Engineering

Safety Administrator

15266

Mason, Ohio

Other Area(s)

BEPC INC. IS LOOKING FOR A SAFETY ADMINISTRATOR IN MASON OHIO!

W2 CONTRACT: 5 MONTHS WITH EXTENSION OR PERMANENCY POSSIBILITIES

PAY:$32.00/Hr. +medical/dental/vision/life insurance

Hours: 60Hrs week.

Need 5 traveling safety admins to start asap.
Multiple locations
100% travel

Position Summary:

Support Project Team in developing and sustaining an Incident and Injury Free Culture (IIFC). Ensure compliance with federal, state, and local safety regulations. Provide technical support and assistance to Project Team in developing and maintaining a Project Safety Roadmap. This position will report to the Director of Installation and Sr. Field Safety Lead.

Essential Job Functions:

• Support Crew Foreman/General Foremen in development of Job Hazard Analyses.

• Evaluate the effectiveness of safety programs through daily field walks. Regulatory compliance and audit oversight.

• Conduct new employee orientation and OSHA 10/ 30 Hour Classes

• Meet regularly with field personnel and support in the development of project specific corrective action plans to address safety issues and concerns

• Provide regular feedback to project leadership in a constructive manner on needed areas for safety improvement and recognition.

• Provide coaching and mentoring for employees exhibiting unsafe behaviors, and provide recognition for employees exhibiting safe behaviors.

• Assist with delivery of job site-specific safety orientations for new employees joining the project, as applicable.

• Assist and co-facilitate safety training, testing for all employees (HazCom, Fall Protection, Lockout/Tag out, etc.)

• Support Project Leadership in the completion of incident investigations.

• Facilitate all injury/illness cases.

• Perform periodic evaluations of power tools and equipment (i.e. scissor lifts, forklifts, fall protection, laser levelers, etc.) to ensure equipment is being maintained in good working order, as applicable.

• Monitor and evaluate CEI/Subcontractor compliance with applicable rules and regulations, and project safety requirements.

• Support Project Leadership in the development and execution of weekly toolbox safety meetings.

• Attend the assigned safety meetings each morning:

• Ensure that meetings are taking place daily

• Audit for continuity of topics to be discussed

• Evaluate the participation of the crew and whether the foreman gave them an opportunity to do so.

• Evaluate meetings and provide feedback to Project Leadership on effectiveness.

• Ensure Foremen, GF and Superintendents are evaluating the job site and giving appropriate coaching as needed

General work environment

• Standing, walking, sitting, climbing, typing, carrying, pushing, and bending for extended periods of time. Work is conducted in both indoor and outdoor constructions job site settings. Environmental conditions will vary.

• Occasional lifting of up to 40 pounds.

• Regularly work at heights and in confined space.

• The duties and responsibilities are intended to describe the general nature and scope of work being performed by this position. This is not a complete listing and other duties will be assigned based on the positions role within the business unit.

Minimum Job Requirements:

• 2 or 4-year college degree desired, preferably in environmental health and safety discipline.

• 5+ years of construction safety experience.

• OSHA 500 Construction required

• Understanding of construction industry standards

• Experience with non-union workforce desired

• CPR/FA Certified

• Ability to work independently, strong communication skills with the ability to influence behaviors

• Proficient in using a computer and Microsoft Office (Outlook, Word, Excel, etc.)

• Safety certification is desired.

Responsible for:

· Identifying hazardous workplace conditions.

· Takes samples and measurements of hazardous materials, and coordinates the removal of physical, biological and chemical hazards.

· Trains employees on safety policies, procedures and regulations.

· Ensures compliance with all applicable federal and state health and safety regulations and ensures necessary records are maintained and prepared according to established guidelines.

· Participates in Occupational Safety and Health Administration (OSHA) inspections, providing inspectors with appropriate documents and identifying safety measures.

· Typically requires a bachelor's degree in area of specialty and 2-4 years of experience in the field or in a related area.

· Familiar with standard concepts, practices, and procedures within a particular field.

· Relies on limited experience and judgment to plan and accomplish goals.

· Performs a variety of tasks.

· Works under general supervision.

· A certain degree of creativity and latitude is required.

· Typically reports to a supervisor.

BEPRO

Date Added: 10-14-2021

Electrical Technician

15265

Princeton, New Jersey

Technical

Research Associate 1

15264

San Diego, California

Manufacturing

Forklift Driver I

15262

Columbus, Ohio

Manufacturing

Medical Device Technician

15261

Temecula, California

Manufacturing

BEPC is in search of a Qualified Medical Device Technician in Temecula, CA!!

Contract W2 Period: 2 Year contract with possibilities for extensions

Pay & Benefits: $17.70/hr. + Medical, Dental, Vision and Life Insurance

Shift is 5a-1:30p/ 6a- 2:30p

Role:

This position is responsible for the production of high quality medical devices within a manufacturing cell.
Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.
Performs routine assignments according to specified and/or standardized procedures.
Work is closely and continually reviewed.
Ensure that relevant job documentation for cell operations and functions is accurate and up to date.
Be able to clearly communicate ideas, problems and solutions to all levels of manufacturing management in both written and oral form.
Maintain a positive attitude when interacting with internal customers and external customers such as tours.
Follow safety guidelines and utilize appropriate safety devices when performing all operations.
Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.
Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Demonstrates a basis understanding of Lean Manufacturing.
Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions -
Understanding of and ability to utilize electronic data collection systems and computer software packages.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to handle and maneuver small components and parts.
Ability to make critical decisions and judgments with minimal supervision.
High school degree or equivalent preferred.

Date Added: 10-14-2021

Assembler II - 2nd Shift

15259

Atlanta, Georgia

Manufacturing

Media Manager

15258

Newark, New Jersey

Marketing

BEPC is seeking a talented Media Manager to join our fast-growing team of consultants in Newark, NJ!

W2 Contract Period: 5+ months with possible opportunities for extensions.

Pay Rate: $41.63/HR plus we offer Medical, Dental, Vision and Life Insurance benefits after 90 days!

Listen up! There’s a revolution afoot in entertainment and education!

We are looking for a results-oriented Media Manager (contractor) in its Marketing team. As a member of the Paid Media organization, you have the opportunity to shape innovative customer-focused programs to drive successful customer acquisition and brand awareness. Your role will focus on managing initiatives specific to new and tentpole Content title releases for the business. The role calls for a media professional who can lead strategy as well as demonstrate expert knowledge of all individual channels from offline to digital. The position will be instrumental in campaign development to launch some of the larger title releases throughout the year involving A-list talent, so a knowledge of the entertainment space is preferred.

The role requires a passion for results, a commitment to action-oriented analysis, an attitude that anything is possible, and a relentless focus on the customer. The right candidate will thrive in a highly entrepreneurial, fast-changing, and collaborative environment where people are driven, enthusiastic, collaborative and not afraid to take risks. Your mission (and ours) is unique and powerful: fill hearts, minds, and souls with premium audio content that enables learning and literate entertainment.

The position’s most critical duties and functions:
A firm grasp of all media channels and how they work within the consumer funnel and drive Entertainment – based launches. Prior experience working on cross-channel strategy
Ownership of spotlight projects from inception of the strategy, to the media approach, to the implementation of the tactics. Ability to interface with and understand the goals of Content Marketing and deliver, in partnership with our agencies, best in class campaigns that help establish us as a premium Entertainment brand
Ability to multi-task across multiple content launches in different phases at the same time. i.e. 1 ready to launch, while 3-4 may be in planning phase. Deep understanding of time needed to deliver winning campaigns on a variety of levels of priority and budgets
Prior experience managing campaign-level budgets
Robust understanding of the digital landscape and channels (mobile, digital, and social). Prior experience with digital campaigns
Expertise in how to drive weekly metrics reports and Paid Media roll-ups. Comfort with digging into the data, and ability to help define new processes when necessary. Analyze regularly distributed analytics reports to better understand what’s working and what’s not and optimize accordingly. Ability to share key insights and data
Day-to-Day agency communication in coordination with all content campaigns
Ability to identify better ways of working at scale through improved processes and changes
BASIC QUALIFICATIONS
Bachelor’s degree in Business, Marketing, Economics, Engineering or a related field of study
8+ years of experience in media, advertising, or marketing
Experience either at an Advertising agency or client side managing media campaigns
Prior ownership of large budgets and forecasting
Strong analytical skills (spreadsheet mastery a must, database experience is a bonus)
Work closely with the various other marketing teams to bring new content to the market
Strong attention to detail with a focus on superior oral and written communication skills
Established track record of creativity and innovation
Ability to drive creative briefing and content delivery when necessary
PREFERRED QUALIFICATIONS
MBA or graduate degree
Proactive and solutions oriented
Entrepreneurial spirit / ability to try different things with minimal direction
Experience in bringing new products to market or launching content/entertainment products

BEPRO

Date Added: 10-14-2021

Rework Position - 2nd Shift

15257

Altavista, Virginia

Other Area(s)

Materials Handler II - 2nd Shift

15255

Irving, Texas

Management

Machine Operator 1 (1st Shift)

15254

San Diego, California

Manufacturing

BEPC INC IS LOOKING FOR A MACHINE OPERATOR IN SAN DIEGO CALIFORNIA !

W2 CONTRACT: 6 MONTHS WITH EXTENSION OR PERMANENCY POSSIBILITIES.

PAY: $17.50/HR+ MEDICAL / DENTAL/ VISION/ LIFE INSURANCE.

HOURS: 6:00 AM to 2:30 PM (mon- fri)

JOB DESCRIPTION:

Under the direction of the Manufacturing Supervisor, the Machine Operator will operate manufacturing equipment according to established specifications, and standard operating procedures and work instructions.

An operator must demonstrate steady progress in learning all equipment and jobs in the assigned manufacturing area.

He/she/They must also exhibit the ability to follow instructions of supervisor while observing the quality of raw and finished goods before, during and after production.

Essential Duties and Responsibilities –

Monitor functions of equipment and operate per documented procedures including maintaining operational logbooks
Provide technicians with symptoms of equipment failures, when required
Assist in Preventative Maintenance (PM) following procedures
Support material handling as necessary
Maintain segregation of materials and lot/receiving numbers
Maintain area in a clean and orderly condition
Adhere to and demonstrate compliance to all company and department standard operating procedures including but not limited to: GMP, device history record, hazard communication and safety rules
Utilize written procedures and training to accomplish tasks noted above
Accept full accountability for product quality
Report to supervisor or management unsolved problems encountered during the workday
Maintain complete and accurate records of work-in-process, component inventories and relative documentation

EDUCATION: HS Diploma or equivalent is required

BEOCS

Date Added: 10-13-2021

Materials Handler II - 2nd Shift

15245

Irving, Texas

Manufacturing

Production Expediter

15242

San Diego, California

Other Area(s)

BEPC INC IS LOOKING FOR A PRODUCTION EXPEDITER IN SAN DIEGO CALIFORNIA !

W2 CONTRACT: 11 MONTHS WITH EXTENSION OR PERMANENCY POSSIBILITIES.

PAY: $25.00/HR+ MEDICAL / DENTAL/ VISION/ LIFE INSURANCE.

HOURS: 40 hrs weekly (mon- fri)

Job Summary
The Production Expeditor serves as the critical connection between the supply chain and manufacturing operations. Critical focus on ensuring adherence to production schedules and identifying process, resources, materials and other gaps that may impact the ability to meet timelines.

Essential Duties and Responsibilities
The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.
• Monitors, evaluates and ensures smooth movement of materials from inventory through the entire production process, from manufacturing to the shipping process.
• Aligns with the weekly and daily manufacturing schedule to ensure 100% on time delivery.
• Ensures production orders have the required materials are on hand in the specified quantity and timeframe in synch with production plans.
• Manage details of production schedule to maximize productivity of manufacturing and shipping departments.
• Serves as a liaison between various departments within the company to ensure production deadlines and schedules are met, ensuring any risks to meeting timelines is acted upon in a timely manner.
• Identify and assist in resolution of scheduling conflicts.
• Ability to remain organized, communicate and solve issues rapidly throughout the production process.
• Provides support to Planners as needed to ensure no negative impact to production and timeline commitments.

Physical Demands
The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
• Sit; use hands to finger, handle or feel objects, tools, or controls.
• Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl.
• Lifting/moving and carrying products weighing up to 40 pounds.
• Exposure to moving mechanical parts, vibration and/or moderate noise levels.
• Exposure to hazardous chemicals or other materials.
• Safety Shoes with Impact and Compression Protection Must be worn.
• Exposure to blood.

Qualifications
Education
• Minimum High School diploma, Associates Degree preferred.

Experience
• Minimum 2 years of related experience in a biotech, life sciences or related industry. Experience or knowledge of the production process, parts and materials required for production. Medical Products Manufacturing GMP, FDA compliance, and ISO experience a plus.

Skills
• Working knowledge of Oracle ERP and MRP required
• Strong organizational and time management skills
• Knowledge of BOMs, routings/recipes and work centers
• Lean/Just in Time concepts, preferred
• Working knowledge of Microsoft Office
• Strong verbal and written communications skills

Date Added: 10-13-2021

Sr Production Control Analyst

15239

Phoenix, Arizona

Other Area(s)

Lead Advanced Engineering Technician - G02550US - AERO E&T -

15238

Clearwater, Florida

Technical

BEPC INC IS LOOKING FOR A LEAD ADVANCED ENGINEERING TECHNICIAN IN CLEARWATER CALIFORNIA!

W2 CONTRACT:6 MONTHS WITH EXTENSION OR PERMANENCY POSSIBILITIES.

PAY: 36.50/HR +MEDICAL/DENTAL/VISION/LIFE INSURANCE

HOURS: 1st, 2nd & 3rd shift - must be willing to work a flexible work schedule as hardware schedule fluctuates. (START DATE ASAP)

Description:
Performs hands-on diverse technical tasks related to testing of advanced electronics assemblies for space and defense applications. This position supports testing, troubleshooting and fault isolation of these assemblies by performing well defined development tests, system integration, and formal acceptance tests, which includes environmental testing. Pro-activeness, good communication skills, and discipline are essential for this position.

This job entails dynamic, thermal, and functional testing. It includes the ability to set-up, program, and operate special test equipment for the program to perform Acceptance Test Procedures. It also requires lifting and handling fixtures as well as the ability to handle and manipulate delicate inertial hardware and circuit card assemblies.

Must be able to keep detailed test logs, follow detailed test procedures without error and provide daily pass-along shift information (both verbal and written documentation).

• Execute on cleanliness/standardization, Safety, equipment/lab maintenance and Operating System tasks on a daily basis; demonstrate commitment to continuous improvement.

• Daily interaction with both test technicians and engineers. Communication and Teamwork skills are extremely important.

Basic Qualifications:
• Associates or technical degree required
• Due to Government regulations, U.S. Citizenship is required.
• Familiar with computers/computer applications (i.e. Word, Excel,)
•
Additional Qualifications:
• Experience with Guidance and Navigation Electronics systems a plus.
• Experience with General Purpose Test Equipment (i.e. as oscilloscopes, spectrum analyzers, and logic analyzers).
• Attention to detail is a must. Ability to follow step-by-step procedures and follow precise instructions
• Environmental test experience is a plus.
• Ability, flexibility and willingness to work different shifts, flex shifts and alternate work weeks including overtime and weekends on a long-term daily basis as business needs require

Preferred skills:
• Technical education is a plus along with a minimum of 4 years experience in an electronics discipline.
• Have an understanding of digital electronics and proficient use of general purpose test equipment such as oscilloscopes and multi-meters along with exposure to environmental testing for space flight products.
• Ability to read schematics, follow procedures, and apply computer skills and technical knowledge to competently troubleshoot and resolve technical problems.
• Capable of generating clear and precise technical documentation for the preparation of action registers, engineering orders, and data book entries.

To start ASAP - If candidate is selected and able to start sooner than requisition the start date will be updated on work order as candidate is needed, sooner than later.

BEPRO

Date Added: 10-12-2021

Marketing Manager of Paid Media

15237

Newark, New Jersey

Marketing

BEPC is seeking 2 skilled Marketing Managers of Paid Media to join our fast-growing team of consultants in Newark, NJ!

W2 Contract Period: 5+ months with possible opportunities for extensions based on business needs and performance.

Pay Rate: $41.63/HR plus we offer Medical, Dental, Vision and Life Insurance benefits after 90 days!

About the Role
We are looking for an experienced manager to help drive the overall business across various media disciplines. The ideal candidate understands the various awareness channels as well as how those tactics best work in complement with performance media, with the ability to bring a holistic, integrated strategy to life. He/she should have a proven track record of strong project management skills, working cross functionally across teams and departments – creative, tech, integrated marketing, etc. The role will be a media generalist working across all tactics and channels. The role will span the general market space as well as the Hispanic space, so a fundamental understanding of the multi-cultural marketplace is preferred. The key responsibilities will include the following:

KEY RESPONSIBILITIES

Flex support across media channels and tactics including Video, Audio, OOH, Mobile App Install, Social, Search and Display
Data collation and analysis of analytics both internally as well as with agencies
Work with real time digital dashboards and distribution to larger team with insights
Help to manage and update budgets and finance documents
Proactive thinking on how to improve process and overall project management
Project management of ad hoc initiatives as well as cross functional work with creative, content, and product

BASIC QUALIFICATIONS

Experience in project management
Preferred experience working with media agencies
Firm understanding of the overall media landscape as we as a comprehensive knowledge of most paid media channels (display, social, radio, TV, OOH, OLV, etc.)
Always up to speed on marketing trends with a keen understanding of ad formats, specifications, and the different tactics
Ability to manage multiple projects at one time in a fast-paced environment
Clear and concise communication skills
Experience in tracking customer journey across multiple devices and provide a holistic view of performance drivers
Strong analytical skills with the ability to draw insights and learnings from reports
Proven ability for innovation and ability to bring new ideas to the table to continue to advance the business
Experience managing a holistic budget

PREFERRED QUALIFICATIONS

4+ years marketing experience in a goal-oriented organization
Experience setting and achieving quantitative goals for both brand and direct response objectives

BEPRO

Date Added: 10-12-2021

Contracts Support Specialist

15233

Marlborough, Massachusetts

Other Area(s)

BEPC is seeking a skilled Contracts Support Specialist to join our fast-growing team of consultants in Marlborough, MA area!

Contract W2 Period: 5 month contract with opportunities for extensions

Pay Rate: $22.00 /HR plus we offer Medical, Dental, Vision and Life Insurance benefits!

This position is responsible to provide timely contract execution, accurate pricing set-up, price discrepancy troubleshooting and root cause resolution across all commercial divisions, using Oracle EBS and SalesForce.

Duties and Responsibilities
• Process contract activations and executions in Contract Management Systems and administer customer pricing in SalesForce and Oracle for assigned product division; enter initial order where appropriate
• Execute best practices for customer contract pricing setup
• Ensure timely research, root cause resolution and respond to pricing inquiries from internal and external customers in specified turn-around time, with weekly credit memo report as one metric to measure success in driving down price discrepancies
• Cross train on other product division requirements to provide back up support to the other Contracts Specialists
• Maintain an understanding of contract requirements to ensure all applicable contract obligations are met in a timely and accurate manner
• Interact directly with internal and external customers, Directors of National Accounts, and field sales regarding contracts (i.e. pricing, products under contract, contract requirement, etc.); provide any ad hoc reports as requested
• Support contract renewal process in partnership with Commercial Contract Specialists
• Collaborate and partner directly with the Corporate Sales organization and where required, provide direct customer interaction to ensure effective contract execution
• Identify continuous improvement opportunities related to the contract activation and execution process
• Work on ad hoc projects as assigned
• Participate in all required job training and development courses and seminars
• Other duties as assigned by Manager

Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the basic knowledge, skills, and/or abilities required.
• Customer focused
• Effective oral and written communication skills are essential
• Outstanding interpersonal skills
• Excellent problem solving and decision making skills
• Ability to exercise initiative and sound judgment in a variety of situations
• Demonstrated ability to meet deadlines under pressure
• Excellent attention to detail
• Strong propensity to learn new software programs/systems
• Ability to interpret and understand complex situations
• Basic accounting or finance understanding; ability to grasp the larger picture/how all pieces interact and affect one another
• Demonstrated ability to work independently with minimal supervision and work well within a team
• Strong communication, interpersonal and organization skills; establishes and builds relationships with stakeholders and cross-functional teams
• Demonstrated ability to maintain a positive attitude and professionalism
• Must be able to work in a fast-paced environment and adapt well to change
• Demonstrated ability to prioritize and multi-task
• Good business acumen
• Ability to interpret contract documents preferred
• Working knowledge of Adobe Standard, and Microsoft Office especially Word, Excel and PowerPoint
• Must be able to work in a fast-paced environment and adapt well to change

Education
• Bachelors degree

Experience
• 3+ years experience in a sales support, contracts support, or legal support role
• Experience working with Oracle or similar system
• Experience working with SalesForce or similar system
• Experience working with and supporting sales and sales contracts in the healthcare industry is strongly preferred
• Experience working with contracts a plus

BEPRO

Date Added: 10-11-2021

Operator III - 2nd Shift

15232

Menlo Park, California

Manufacturing

W2 contract period 12 months
Pay rate: $24.76

Description

This position is responsible for the production of high quality cardiovascular medical devices on a team within a manufacturing cell.
This position includes detailed assembly and operation of various equipment and machinery per documented procedures.
This may include electronic assembly, casting/coating functions, mechanical assembly, and packaging.
Cleans tools and equipment per documented procedures.
Disposes hazardous waste material on corresponding hazardous waste areas.

Duties

Assembles medical devices and related components. Depending on work area, it may be a controlled cleanroom environment.
May include use of microscopes, use of hand tools, razor blades, syringes, soldering, adhesive bonding, and operating various equipment.
Performs routine assignments according to specified and/or standardized procedures.
Work is closely and continually reviewed.
Performs visual inspection and precision measurements on components and assemblies.
Performs tests on units using computerized test equipment.
Repairs and corrects devices/components using microscopes and applicable tools.
Packages devices ensuring all parts are accurate and documentation is complete.
Maintains accurate records to ensure travelers, shop floor paperwork and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Follows safety guidelines and utilize appropriate safety devices and equipment when performing all operations.
Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics.
Notifies supervisor or lead of the need to replenish supplies/materials and of any production difficulties that cannot be readily corrected.
Participates with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations. Cooperates in keeping a clean, sanitary work environment throughout the building.
Performs other related duties as directed or assigned.

Requirements:

Must be able to read, comprehend and follow English written procedures at a 6th grade level.
Must have good basic math skills at a 6th grade level.
Must be able to speak, follow verbal instructions and communicate effectively in English.
Possesses understanding of and ability to utilize electronic data collection systems and computer software packages.
Must have good dexterity to handle and maneuver small components and parts.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to make critical decisions and judgments with minimal supervision.
High school diploma required
2+ years of experience

BEOCS

Date Added: 10-11-2021

Operator II - 2nd Shift

15230

Menlo Park, California

Manufacturing

Mon – Fri (3pm – 1:30am)

OT Paid Time and a Half

This position is responsible for the production of high quality cardiovascular medical devices on a team within a manufacturing cell. This position includes detailed assembly and operation of various equipment and machinery per documented procedures. This may include electronic assembly, casting/coating functions, mechanical assembly, and packaging. Cleans tools and equipment per documented procedures. Disposes hazardous waste material on corresponding hazardous waste areas

Duties & Responsibilities:

Assembles medical devices and related components
Depending on work area, it may be a controlled cleanroom environment
May include use of microscopes, use of hand tools, razor blades, syringes, soldering, adhesive bonding, and operating various equipment
Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed
Performs visual inspection and precision measurements on components and assemblies. Performs tests on units using computerized test equipment
Repairs and corrects devices/components using microscopes and applicable tools
Package’s devices ensuring all parts are accurate and documentation is complete
Maintains accurate records to ensure travelers, shop floor paperwork and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products
Follows safety guidelines and utilize appropriate safety devices and equipment when performing all operations
Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics
Notifies supervisor or lead of the need to replenish supplies/materials and of any production difficulties that cannot be readily corrected
Participates with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations
Cooperates in keeping a clean, sanitary work environment throughout the building
Performs other related duties as directed or assigned

Requirements:

Verbal and Written Communication
Must have good basic math skills
Possesses understanding of and ability to utilize electronic data collection systems and computer software packages
Must have good dexterity to handle and maneuver small components and parts
Ability to prioritize and manage their time effectively
Ability to make critical decisions and judgments with minimal supervision

Education & Experience:

High school diploma required
2+ years of experience

BEOCS

Date Added: 10-11-2021

Operator II

15229

Menlo Park, California

Manufacturing

BEPC is looking for a confident Assembly Technician to come join our fast-growing team in Menlo Park, CA!

Contract W2 period: 12-month contract with possibilities for extensions

Pay: $21.50 (BONUS AFTER 2 MONTHS)

Shift: 4am-2:30pm

Job Description:
This position is responsible for the production of high quality cardiovascular medical devices on a team within a manufacturing cell.

This position includes detailed assembly and operation of various equipment and machinery per documented procedures.
This may include electronic assembly, casting/coating functions, mechanical assembly and packaging.
Cleans tools and equipment per documented procedures.
Disposes hazardous waste material on corresponding hazardous waste areas.

Duties

Assembles medical devices and related components.
Depending on work area, it may be a controlled cleanroom environment.
May include use of microscopes, use of hand tools, razor blades, syringes, soldering, adhesive bonding, and operating various equipment.
Performs routine assignments according to specified and/or standardized procedures.
Work is closely and continually reviewed.
Performs visual inspection and precision measurements on components and assemblies.
Performs tests on units using computerized test equipment.
Repairs and corrects devices/components using microscopes and applicable tools.
Packages devices ensuring all parts are accurate and documentation is complete.
Maintains accurate records to ensure travelers, shop floor paperwork and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Follows safety guidelines and utilize appropriate safety devices and equipment when performing all operations.
Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics.
Notifies supervisor or lead of the need to replenish supplies/materials and of any production difficulties that cannot be readily corrected.
Participates with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Cooperates in keeping a clean, sanitary work environment throughout the building.
Performs other related duties as directed or assigned.

Requirements:

Must be able to read, comprehend and follow English written procedures at a 6th grade level.
Must have good basic math skills at a 6th grade level.
Must be able to speak, follow verbal instructions and communicate effectively in English.
Possesses understanding of and ability to utilize electronic data collection systems and computer software packages.
Must have good dexterity to handle and maneuver small components and parts.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to make critical decisions and judgments with minimal supervision.
High school diploma required
2+ years of experience

BEOCS

Date Added: 10-11-2021

Operator I - 2nd Shift

15228

Menlo Park, California

Manufacturing

"This is a non-exempt position.
This position is responsible for the production of high quality medical devices within a manufacturing cell. Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.

Performs routine assignments according to specified and/or standardized procedures.
Work is closely and continually reviewed.
Ensure that relevant job documentation for cell operations and functions is accurate and up to date.
Be able to clearly communicate ideas, problems and solutions to all levels of manufacturing management in both written and oral form.
Maintain a positive attitude when interacting with internal customers and external customers such as tours.
Follow safety guidelines and utilize appropriate safety devices when performing all operations.
Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.
Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Demonstrates a basis understanding of Lean Manufacturing.
Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions - Understanding of and ability to utilize electronic data collection systems and computer software packages.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to handle and maneuver small components and parts. Ability to make critical decisions and judgments with minimal supervision.
High school degree or equivalent preferred.

Date Added: 10-11-2021

Operator I

15227

Menlo Park, California

Manufacturing

"This is a non-exempt position.
1st shift pay $20.00 -
2nd shift pay $20.00
This position is responsible for the production of high quality medical devices within a manufacturing cell. Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.

Performs routine assignments according to specified and/or standardized procedures.
Work is closely and continually reviewed.
Ensure that relevant job documentation for cell operations and functions is accurate and up to date.
Be able to clearly communicate ideas, problems and solutions to all levels of manufacturing management in both written and oral form.
Maintain a positive attitude when interacting with internal customers and external customers such as tours.
Follow safety guidelines and utilize appropriate safety devices when performing all operations.
Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.
Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Demonstrates a basis understanding of Lean Manufacturing.
Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions - Understanding of and ability to utilize electronic data collection systems and computer software packages.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to handle and maneuver small components and parts. Ability to make critical decisions and judgments with minimal supervision.
High school degree or equivalent preferred.

Date Added: 10-11-2021

Director, Project Management

15225

Newark, New Jersey

Project Management

BEPC is seeking a talented Director, Project Management to join our fast-growing team of consultants in Newark, NJ!

W2 Contract Period: 5+ months with possible opportunities for extensions based on business needs and performance.

Pay Rate: $60.87/HR plus we offer Medical, Dental, Vision and Life Insurance benefits after 90 days!

The Integrated Marketing team is looking for a Director of Project Management to own and drive the execution Marketing Campaigns into the marketplace. Together, we’ll develop marketing programs, creative assets, and experiences that help build and extend our brand, attract, and convert new customers, and engage our existing community of listeners in authentic and compelling ways.

ABOUT YOU

You are a skilled Project Management professional who is detail oriented, have an obsessive need for order, and find pleasure in running the show
You are a master juggler, momentum builder, facilitator, diplomat, and project champion
You can connect the dots across a multitude of different but inter-connected areas
You are data driven and operationally grounded. You are comfortable speaking your mind and presenting a recommendation based on data and your previous experience

KEY RESPONSIBILITIES

Work collaboratively with creative and marketing teams to project manage small to large-scale creative projects, ensuring completion on time and budget
Develop comprehensive project plans with milestones and schedules, ensuring project team and stakeholder alignment
Use and continually develop leadership skills to help distill and translate complex information into clear takeaways and actions for the creative team
Lead communications around project priorities to the creative team
Understand and identify key inter-dependencies and critical path tasks, as well as anticipate potential issues.
Track project performance, specifically to analyze the successful completion of short- and long-term goals
Proactively keep team members on deadlines in an effective but positive way.
Communicate project statuses, flagging and troubleshooting issues, escalating ones that require attention with proposals of next steps / solutions
Support vendor relationships (including ongoing project communications as well as financial areas such as purchase order and invoice management.)
Track and balance resource utilization and creative team capacity
Effectively manage junior members of the production team
Research and implement new tools, workflows and processes as needed

BASIC QUALIFICATIONS

Strong organizational and time management skills with ability to set priorities, multi-task, and meet deadlines in a fast-paced environment
Self-starter attitude and ability to build a strong rapport and trust with resources across multiple functional areas
Excellent organizational and project management skills with experience managing multiple projects with competing priorities in a calm and efficient manner
Experience managing creative development
Knows project management principles, processes, and tools
10+ years of Marketing experience preferably with a Global company
5+ years project management experience preferably at a creative agency, entertainment company or network
Strong written & oral communication and presentation skills
Bachelor's degree or equivalent

BEPRO

Date Added: 10-11-2021

Technical Writer 1

15223

San Diego, California

Other Area(s)

Lead System Engineer

15221

Phoenix, Arizona

Engineering

BEPC has an open position for a Lead System Engineer in Phoenix, AZ!!

Contract W2 Period: 8 month contract with possibilities for extensions
Pay & Benefits: $57/hr. + Medical, Dental, Vision and Life Insurance

????

This position requires knowledge and experience with requirements management principles.
Key Responsibilities - Leads Engineering team through System Verification activities to satisfy all customer requirements.
Coordinates Requirements Based Engineering standards for the project and drives Engineering team to follow the standards.
Works directly with subject matter experts and authors of analysis and testing documents to coordinate verification activities that return the necessary data for customer requirements verification.
Oversees the configuration management of the customer requirements document and uses the joint change control board process to control customer requirements changes.
MUST HAVE
Bachelors Degree in Engineering
At least 8 years of demonstrated experience leading engineering teams in a dynamic multi-functional environment
Due to export control regulations, this position requires US citizenship status.
We value individuals who are self-motivated and able to work with little supervision, who consistently take the initiative to get things done, do things before being asked by others or forced to by events.
Ability to multi-task and manage multiple work streams to answer system level verification questions and to close all disconnects between customer requirements and verification activities.
Experience working with external customers.
Experience using IBM Rationale DOORs for requirements tracking and traceability.
Experience with aerospace system development standards like SAE ARP4754A and DO-178C is a plus.

BEOCS

Date Added: 10-11-2021

Operator III

15220

Temecula, California

Manufacturing

BEPC INC IS LOOKING FOR MEDICAL DEVICE ASSEMBLER III IN TEMECULA CALIFORNIA!

W2 CONTRACT: 2 years with extension or permanency possibilities.

PAY: $18.25/hr + Medical dental vision and life insurance.

HOURS: 7 am to 4:30 pm (M-F)

JOB DESCRIPTION:

DUTIES MAY INCLUDE:

Electronic assembly, casting/coating functions, mechanical assembly and packaging.
Cleans tools and equipment per documented procedures. Disposes hazardous waste material on corresponding hazardous waste areas.
Assembles medical devices and related components.
Depending on work area, it may be a controlled cleanroom environment.
Use of microscopes, use of hand tools, razor blades, syringes, soldering, adhesive bonding, and operating various equipment.
Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed.
Performs visual inspection and precision measurements on components and assemblies.
Performs tests on units using computerized test equipment. Repairs and corrects devices/components using microscopes and applicable tools.
Packages devices ensuring all parts are accurate and documentation is complete.
Maintains accurate records to ensure travelers, shop floor paperwork and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Follows safety guidelines and utilize appropriate safety devices and equipment when performing all operations.
Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics.
Notifies supervisor or lead of the need to replenish supplies/materials and of any production difficulties that cannot be readily corrected.
Participates with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Cooperates in keeping a clean, sanitary work environment throughout the building.
Performs other related duties as directed or assigned.

REQUIREMENTS:

Must be able to read, comprehend and follow English written procedures at a 6th grade level.
Must have good basic math skills at a 6th grade level.
Must be able to speak, follow verbal instructions and communicate effectively in English.
Possesses understanding of and ability to utilize electronic data collection systems and computer software packages.
Must have good dexterity to handle and maneuver small components and parts.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to make critical decisions and judgments with minimal supervision.

EDUCATION: High school diploma required 5+ years of experience.

BEOCS

Date Added: 10-11-2021

Operator II

15219

Temecula, California

Manufacturing

Medical Device Technician

15218

Temecula, California

Manufacturing

BEPC is in search of a Qualified Medical Device Technician in Temecula, CA!!

Contract W2 Period: 2 Year contract with possibilities for extensions

Pay & Benefits: $17.70/hr. + Medical, Dental, Vision and Life Insurance

Shift is 7:30a-4:30p

Role:

This position is responsible for the production of high quality medical devices within a manufacturing cell.
Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.
Performs routine assignments according to specified and/or standardized procedures.
Work is closely and continually reviewed.
Ensure that relevant job documentation for cell operations and functions is accurate and up to date.
Be able to clearly communicate ideas, problems and solutions to all levels of manufacturing management in both written and oral form.
Maintain a positive attitude when interacting with internal customers and external customers such as tours.
Follow safety guidelines and utilize appropriate safety devices when performing all operations.
Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.
Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Demonstrates a basis understanding of Lean Manufacturing.
Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions -
Understanding of and ability to utilize electronic data collection systems and computer software packages.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to handle and maneuver small components and parts.
Ability to make critical decisions and judgments with minimal supervision.
High school degree or equivalent preferred.

BEOCS

Date Added: 10-11-2021

Operator II

15217

Temecula, California

Manufacturing

Operator III

15216

Temecula, California

Manufacturing

BEPC INC IS LOOKING FOR MEDICAL DEVICE ASSEMBLER III IN TEMECULA CALIFORNIA!

W2 CONTRACT: 2 years with extension or permanency possibilities.

PAY: $18.25/hr + Medical dental vision and life insurance.

HOURS: 7 am to 4:30 pm (M-F)

JOB DESCRIPTION:

DUTIES MAY INCLUDE:

Electronic assembly, casting/coating functions, mechanical assembly and packaging.
Cleans tools and equipment per documented procedures. Disposes hazardous waste material on corresponding hazardous waste areas.
Assembles medical devices and related components.
Depending on work area, it may be a controlled cleanroom environment.
Use of microscopes, use of hand tools, razor blades, syringes, soldering, adhesive bonding, and operating various equipment.
Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed.
Performs visual inspection and precision measurements on components and assemblies.
Performs tests on units using computerized test equipment. Repairs and corrects devices/components using microscopes and applicable tools.
Packages devices ensuring all parts are accurate and documentation is complete.
Maintains accurate records to ensure travelers, shop floor paperwork and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Follows safety guidelines and utilize appropriate safety devices and equipment when performing all operations.
Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics.
Notifies supervisor or lead of the need to replenish supplies/materials and of any production difficulties that cannot be readily corrected.
Participates with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Cooperates in keeping a clean, sanitary work environment throughout the building.
Performs other related duties as directed or assigned.

REQUIREMENTS:

Must be able to read, comprehend and follow English written procedures at a 6th grade level.
Must have good basic math skills at a 6th grade level.
Must be able to speak, follow verbal instructions and communicate effectively in English.
Possesses understanding of and ability to utilize electronic data collection systems and computer software packages.
Must have good dexterity to handle and maneuver small components and parts.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to make critical decisions and judgments with minimal supervision.

EDUCATION: High school diploma required 5+ years of experience.

BEOCS

Date Added: 10-11-2021

Environmental Health and Safety Technician

15212

Hillsboro, Oregon

Manufacturing

***Contract duration 6 months with possible extensions up to 3 years Onsite 5 days a week, 40 hours a week***

The individual hired for this position will be part of the Safety, Health, and Environmental (SHE) team and will assist with the completion of the Hillsboro, Oregon site SHE goals and objectives. This will include the development and implementation of SHE programs, working on closure of gaps identified, the initiation and completion of improvement projects, in addition to assisting with the resolution of SHE concerns from our manufacturing customers.

Responsibilities:

• Develop and implement SHE management systems to drive compliance with safety and environmental regulations
• Perform and guide activities related to all site SHE programs including Ergonomics, Personal Protective Equipment, Fall Protection, Lock-Out Tag-Out (LOTO), Machine Guarding, Confined Spaces, Contractor Safety, and Hazard Communication
• Communicate effectively with our customers employing the ability to present ideas well one on one in small groups and to larger audiences
• Effectively influence others to take action to mitigate SHE risks
• Conduct ergonomic risk assessments to systematically identify and reduce risk of work related musculoskeletal disorders, includes both office and manufacturing setups
• Conduct inspections and job hazard (risk) analyses
• Identify and implement corrective and preventative actions
• Assist in investigation of SHE incidents and development of corrective actions
• Apply engineering principles to reduce SHE risks and Strengthen Compliance
• Develop appropriate engineering or work process modifications to prevent worker illness or injury
• Provide SHE assistance and guidance to safety committees, including EHS regulatory interpretations
• Provide SHE support in the design and installation of new or modified equipment and management of change processes
• Develop content and present SHE training to plant employees
• Provide SHE assistance to Value Streams Qualifications and Requirements
• Bachelor’s degree with minimum 3 years of SHE experience in manufacturing and/or consulting environments or a combination of equivalent education and experience.
• Experience with implementing and or managing an industrial ergonomics program
• Work effectively with multiple levels of employees
• Well-developed planning and organizational skills including the ability to prioritize activities, meet commitments, and proactively manage time and a challenging workload
• Utilize approaches that require innovation and change.
• Well-developed planning and organizational skills including the ability to prioritize activities, meet commitments, and proactively manage time and a challenging workload.
• Demonstrates clear and concise oral and written skills as well as an ability to train others.
• Effective listening skills.
• Proactively support and/or lead EHS initiatives that support the business.
• Strong computer skills

BEOCS

Date Added: 10-08-2021

Senior Electrical Engineer

15211

Westford, Massachusetts

Engineering

BEPC has an open position for a Senior Electrical Engineer in Westford, MA!

Contract W2 Period: 6 month contract with possibilities for extensions
Pay & Benefits: $62/hr. + Medical, Dental, Vision and Life Insurance

Bachelor’s Degree in electrical engineering (BSEE) with 5+ years of experience in Medical Device required.
Knowledge of IEC 60601-1, 3.1 edition Safety and Essential performance and IEC60601-1-2 4th edition Electromagnetic disturbances.
Experience testing and verifying complex electrical systems.
This position will be On-site; occasional local travel (destinations within 30 minutes from office in Westford, MA).
Infrequent remote travel (west coast USA)
Skills: Relevant work experience in performing the layout, construction, and evaluation of a variety of prototype Printed Circuit Boards, fixtures and tools.
Demonstrated ability to develop new design features as part of existing systems.
Documented record of delivering tool engineering information which adds value to
managements decision making process. Demonstrated ability to understand and comply with applicable FDA regulations and
Company operating procedures, processes, policies and tasks. Advanced personal computer skills, including spreadsheet, word processing, database management, and specialized applications.
Advanced credential or professional certification in a relevant discipline/concentration desired.
Six-Sigma knowledge and experience desired.
Training and experience in manufacturing processes and methods desired, especially in the manufacturing of medical devices.
Experience working in a broader enterprise/cross-division business unit model preferred.
Ability to work in a highly matrixed and geographically diverse business environment.
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
Ability to leverage and/or engage others to accomplish projects.
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
Multitasks, prioritizes and meets deadlines in timely manner.
Strong organizational and follow-up skills, as well as attention to detail.
Ability to travel approximately 10%, including internationally.
Duties: Lays out and constructs a variety of prototype tools and fixtures required for development purposes..
Conducts evaluations, tests and analyses related to feasibility and function.
Performs troubleshooting and fault isolation activities on a variety of breadboards and hybrids.
Conducts measurements specified in design verification plans, documents and tabulates results, and provides engineering test reports.
Documents custom tools with specifications, schematics and mechanical layouts to support document control and tool release.
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
QUALIFICATIONS Education Level Bachelors Degree in Electrical Engineering or related Engineering field"

BEOCS

Date Added: 10-08-2021

Materials Coordinator

15207

Dayton, Ohio

Other Area(s)

Validation Engineer

15206

Vacaville, California

Engineering

BEPC has an open position for a Validation Engineer in Vacaville, CA!

Contract W2 Period: 3 year contract with possibilities for extensions
Pay & Benefits: $51.67/hr. + Medical, Dental, Vision and Life Insurance

Description:

Primarily responsible for the support and execution of laboratory equipment qualification and associated computer system validation activities in compliance with current cGMP regulations and corporate principles, quality policies, standards, and core values. You will work closely with instrument vendors, facilities, IT and lab personnel to coordinate the acquisition, installation, qualification, and periodic review of laboratory instruments.

Perform qualification of laboratory equipment in accordance with EQ policies, plans and procedures.
Coordinate with laboratory personnel to define qualification requirements.
Author, review and execute equipment qualification protocols.
Coordinate equipment qualification activities with vendors and other support groups.
Coordinate equipment maintenance activities with vendors and other support groups, as required.
Identify business, quality, and compliance gaps and propose and implement potential improvements to systems and procedures
Collaborate and author department policies and procedures.
Sign documents for activities as authorized and described by corporate policies, procedures and job descriptions.
Provide input to technical / investigation reports.
Identify, troubleshoot, and propose resolution to technical problems.
Identify gaps in and potential improvements to systems and procedures.
Receive and provide training.
Provide input to and participate in assay transfer/validation associated with equipment qualification/lifecycle.
Coordinate with customers to support multi-site operational activities.
Present equipment lifecycle and associated procedures/material during internal and external audits and regulatory inspections.
Works to meet schedules and set timelines.
Participate in and/or lead group project teamwork; project and process improvements.
Perform other duties as requested by managers to support Quality activities.

BEOCS

Date Added: 10-08-2021

Product Owner - Data Analytics

15205

East Hanover , New Jersey

Professional

BEPC Inc is looking for a Product Owner – Data Analytical in East Hanover, NJ!
Contract W2 Period: 1 year contract with possibilities for extensions
Pay & Benefits: $40/hr. +Medical, Dental, Vision and Life Insurance

Duties:

This is not a project manager. This person is a "product owner" and must have experience with SAFe, scrum or agile experience.
Serve as a voice to project the expectations of customers on new or already existing products
Highlight product features in a manner clearly understandable to the development team
Manage and develop product backlog, as well as user stories backlog for implementation
Conduct backlog grooming meetings with a team of product owners
Attend sprint planning and demo meetings to give feedback on sprint achievement, as well as to scrum team
Monitor the progress of product development, as well as plan for product release
Contact customers and end users to obtain information on expected product features
Provide reports to update management and stakeholders on product development operations
Analyze customer opinions and feedback to determine features or components that will add good value to a product
Participate in agile conferences and study relevant scrum material to update job knowledge/skill
Constantly exchange ideas with product owners within an organization
Assess product value stream to identify areas that require improvements
Measure product performance as well as value delivered to clients in order to make adjustments where necessary
Develop and implement action plans for building and sustaining demand for a product
Ensure implemented product features add value to end users and increase company returns.

Skills:

Healthcare experience preferred
Web application and/or salesforce.com experience preferred
Product owners are able to direct and motivate the product development team of an organization
They are able to conduct surveys to determine most appropriate feature to add to a new or existing product
They are adept to working with user groups and scrum team to obtain and analyze user stories.

Education:

Bachelor's degree in Software engineering, business management or related disciplines.
Training and certification as a professional scrum product owner (PSPO) or as a certified scrum product owner (CSPO) is also crucial for the position

Additional skills:

CSPO
Big data
BI -Qlik
Technical Lead to Product owner transition Fast paced & team player
HEALTHCARE PROJECT MANAGEMENT
PROJECT MANAGEMENT
ENGINEERING PROJECT MANAGEMENT
AGILE PDM
Agile
Candidate should be local within NY/NJ for potential to come on campus.

BEOCS

Date Added: 10-08-2021

Scrum Product Owner - Healthcare / Pharmaceuticals

15203

East Hanover, New Jersey

IT/Software Development

Duties:

Serve as a voice to project the expectations of customers on new or already existing products
Highlight product features in a manner clearly understandable to the development team
Manage and develop product backlog, as well as user stories backlog for implementation
Conduct backlog grooming meetings with a team of product owners
Attend sprint planning and demo meetings to give feedback on sprint achievement, as well as to scrum team
Monitor the progress of product development, as well as plan for product release
Contact customers and end users to obtain information on expected product features
Provide reports to update management and stakeholders on product development operations
Analyze customer opinions and feedback to determine features or components that will add good value to a product
Participate in agile conferences and study relevant scrum material to update job knowledge/skill
Constantly exchange ideas with product owners within an organization
Assess product value stream to identify areas that require improvements
Measure product performance as well as value delivered to clients in order to make adjustments where necessary
Develop and implement action plans for building and sustaining demand for a product
Ensure implemented product features add value to end users and increase company returns.

Skills:

Healthcare experience preferred
Web application and/or salesforce.com experience preferred Leadership

Skill:

Product owners are able to direct and motivate the product development team of an organization

Analytical Skill:

They are able to conduct surveys to determine most appropriate feature to add to a new or existing product Interpersonal

Skill:

They are adept to working with user groups and scrum team to obtain and analyze user stories.

Education:

Bachelor's degree in Software engineering, business management or related disciplines.
Training and certification as a professional scrum product owner (PSPO) or as a certified scrum product owner (CSPO) is also crucial for the position

Required Skills:

HEALTHCARE PROJECT MANAGEMENT
PROJECT MANAGEMENT
ENGINEERING PROJECT MANAGEMENT
AGILE PDM
Agile
Scrum

BEOCS

Date Added: 10-07-2021

Processing Operator I

15202

Casa Grande, Arizona

Manufacturing

Receipt Inspection Tech

15201

Scarborough, Maine

Technical

BEPC Inc is looking for a Receipt Inspection Tech to join our fast growing team of consultants in the Scarborough, Maine area!

Contract W2 Period: 2 months with possibility of extension

Pay/Benefits: $23.70/hour

40 hours per week / Mon-Fri 8 am - 5 pm / Overtime will be paid at time and a half

Job Description:

Performs work required to ensure incoming material quality is maintained at standards set forth by the Company. The focused areas include incoming inspection, testing, auditing, and documentation of materials purchased.

Essential Duties and Responsibilities include the following. Other duties may be assigned.

Perform incoming testing for purchased materials.
Manage discrepant material process for materials not meeting performance criteria.
Maintain all laboratory equipment.
Calibrate appropriate QC laboratory equipment according to schedule
Work to ensure incoming materials are released on time and according to schedule.
Assist Supervisor/Manager in troubleshooting and other projects as necessary.
Provide support with technical and quality issues as needed.
Perform gauge R&R's and other inspection method qualifications as required.
Provide input and assist in updating SOPs.
Maintain area compliance per FDA, ISO and OSHA requirements.

This job has no supervisory responsibilities.

Education and/or Experience

High school diploma or general education degree (GED); or one to three months related experience and/or training; or equivalent combination of education and experience.
ASQ certified inspector desired. Minimum two years experience in a regulated industry desired. One to three years experience in Quality Control is desired.

Language Skills

Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization.

Mathematical Skills

Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.

Reasoning Ability

Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations.

Computer Skills

To perform this job successfully, an individual should have knowledge of Inventory software; Spreadsheet software and Word Processing software.

Skills and Abilities

Ability to use measurement equipment
Ability to follow procedures and accurately document results
Knowledge of gauging and metrology
Knowledge and experience with inventory management systems

Other Qualifications
Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is frequently required to stand; walk and talk or hear. The employee is occasionally required to sit; use hands to finger, handle, or feel; reach with hands and arms and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include color vision.

Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be
made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this Job, the employee is occasionally exposed to moving mechanical parts; toxic or caustic chemicals and risk of electrical shock. The noise level in the work environment is usually quiet.

BEOCS

Date Added: 10-07-2021

Machine Operator 1 (1st Shift)

15199

San Diego, California

Manufacturing

BEPC Inc. is urgently searching for a Machine Operator I in San Diego, CA.

W2 CONTRACT: 7-month contract with opportunities for extensions.

PAY AND BENEFITS: $17.50/ hr. + Medical, Dental, Vision and Life Insurance.

SCHEDULE: 1^st Shift 6:30 a.m. – 2:30 p.m.

Job description:

Perform well in a team environment
Take initiative to help their teammates
Motivated to do excellent work every day
Machine Operator will operate manufacturing equipment according to established specifications, and standard operating procedures and work instructions.
Must demonstrate steady progress in learning all equipment and jobs in the assigned manufacturing area.
Must also exhibit the ability to follow instructions of supervisor while observing the quality of raw and finished goods before, during and after production.
Monitor functions of equipment and operate per documented procedures including maintaining operational logbooks.
Provide technicians with symptoms of equipment failures, when required.
Assist in Preventative Maintenance (PM) following procedures.
Support material handling as necessary.
Maintain segregation of materials and lot/receiving numbers.
Maintain area in a clean and orderly condition.
Adhere to and demonstrate compliance to all company and department standard operating procedures including but not limited to: GMP, device history record, hazard communication and safety rules.
Utilize written procedures and training to accomplish tasks noted above.
Accept full accountability for product quality.
Report to supervisor or management unsolved problems encountered during the workday.
Maintain complete and accurate records of work-in-process, component inventories and relative documentation.

BEOCS

Date Added: 10-07-2021

Segmentation & Insights Manager

15197

Newark, New Jersey

Marketing

BEPC is seeking a talented Segmentation & Insights Manager to join our fast-growing team of consultants in Newark, NJ!

W2 Contract Period: 5+ months with possible opportunities for extensions based on business needs and performance!

Pay Rate: $41.63/HR plus we offer Medical, Dental, Vision and Life Insurance benefits after 90 days!

The Marketing Operations team is looking for a sharp, technically capable and data-focused Manager to help support customer segmentation efforts and reporting on campaign performance and email/push channel health metrics. This role will have the opportunity to shape innovative customer-focused programs designed to deepen member relationships and enhance acquisition efforts. The ideal candidate must be a creative problem solver who can partner closely with business owners to support a customer-focused marketing strategy, and who can provide data-driven insights into campaign performance and channel health metrics.

KEY RESPONSIBILITIES

Support Marketing and other stakeholder teams with sophisticated campaign targeting and segmentation capabilities
Maintain and develop segmentation for automated programs (onboarding, retention, etc.)
Ensure segmentation supports testing strategies that allow for accurate measurement of campaign performance
Partner with Marketing and Business Intelligence stakeholders to assess campaign performance and make recommendations for optimizing future efforts
Collaborate with Technology partners on data integration initiatives in support of new targeting, segmentation, and personalization capabilities
Partner with Tech and Data Engineering teams to diagnose and drive resolution of technical issues relating to customer targeting and data hygiene

BASIC QUALIFICATIONS

Minimum of 3 years in CRM, Database or Campaign Analytics roles
Advanced knowledge of SQL (experience with AWS Redshift a plus)
Experience supporting outbound marketing teams, generating audiences for email and mobile push notifications and ensuring segmentation supports campaign testing strategies (e.g., proper sampling techniques and sizing of treatment and control groups)
Experience creating segments in support of multi-channel campaigns and automated customer journeys
Must be familiar with customer attributes and outbound campaign data (email, push)
Technically capable with excellent verbal and written communication skills
Strong analytical capability and a solid understanding of campaign performance and channel health metrics
Proficient knowledge of MS Office applications (esp. Excel and PowerPoint)
Bachelor’s degree in Business, Marketing, Computer Science, Engineering or a related field of study

PREFERRED QUALIFICATIONS

Experience working in Jira or similar workflow management software
Knowledge of email and mobile push marketing best practices
Familiarity with statistical modeling and associated tools/programs
Familiarity with email/push testing and optimization platforms (Movable Ink, Persado)
E-commerce experience (including prior experience with membership- or subscription-based businesses in a B2B or B2C industry

BEPRO

Date Added: 10-07-2021

Supplier Quality Engineer - Entry

15196

Scarborough, Maine

Engineering

BEPC is looking for a confident Supplier Quality Engineer to come join our fast-growing team in Scarborough, ME!

Contract W2 period: 5-month contract with possibilities for extensions

Pay: $37.75/hour

Shift: 8am-5pm

Job Description:

Drives improvement and corrective action in the quality of components sourced from outside suppliers.
Provides technical support in the selection of suppliers.
Develops acceptance criteria for materials.
Monitors supplier performance to drive supplier corrective action, manufacturing yield issues and field failures.
Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
Develop corrective action plan where necessary.
Will perform this job in a quality system environment.
Failure to adequately perform tasks can result in noncompliance with governmental regulations.
May lead a project team of moderate scope.
Provides guidance to less experienced staff.

Responsibilities:

Assess potential new suppliers for technical, quality and manufacturing capabilities. Provides technical support for the introduction of components from a new supplier.
Generates and maintains incoming inspection procedures. Trains inspectors to these procedures.
Develops and/or sources inspection tools and equipment.
Assists in generating component specifications.
Generate test protocols, monitor testing, issue qualification test reports and approve components for use in products.
Provide input to Design Engineering on new component technology and assist in component selection with quality and reliability analysis.;
Analyzes incoming material defects. Dispositions and drives corrective action as necessary. Communicates issues to suppliers.
Reviews new design specifications and provides input from component quality and manufacturability perspective.
Investigates field failures related to supplier materials.

Requirements:

BS degree in engineering or related scientific field plus 0-4 years of related work experience with a good understanding of specified functional area, or Master's degree with 0-2 years of related work experience.

BEOCS

Date Added: 10-07-2021

Quality Control Technician

15195

Westbrook, Maine

Technical

Summary
Perform a wide variety of activities to support the Quality Management System.

Essential Duties and Responsibilities
• Conduct product testing, including testing to support complaint investigations and stability verification
• Generate product testing results reports
• Review production batch records (DHR's) for accuracy and completeness in order to approve intermediate products for use in production. Review finished goods batch records. Report all deviations in these records and assures these have been addressed and resolved prior to issuing approval.
• Conduct spot-check inspections/audits of production operations
• Participate in the internal audit program
• Write, review and approve Standard Operating Procedures (SOPs) as necessary
• May assist in supporting the Document Control program, record retention areas, and sample retention areas

• May support returned instrument processing:
o Log returned instruments from the field.
o Decontaminate returned instruments in a Biohazard level II environment following standard operating procedure and documenting decontamination as required.
o Inspect returned instruments for damage, and performing basic investigation and documenting results prior to second level processing.
o As necessary, process instrument documentation for return to repair facility, and pack instruments as required.

Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP)

Education and/or Experience
Bachelor's degree in a scientific or technical area or equivalent combination of experience and education. At least one year in quality assurance role in medical device industry is preferred.

Language Skills
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before small groups of customers or employees of organization.

Mathematical Skills
Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.

Computer Skills
To perform this job successfully, an individual should have knowledge of Database software; Internet software; Inventory software; Spreadsheet software and Word Processing software.

Other Skills and Abilities
Ability to follow procedures and accurately document results
Understanding the manufacturing processes of Company products and ability to recognize deviations from approved documented procedures
Attention to detail.
Ability to use bleach for cleaning purposes is required.

Physical Demands
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this Job, the employee is regularly required to sit and stand. The employee is occasionally required to walk.

Work Environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

The noise level in the work environment is usually quiet.

Comments
Shift: Fri-Mon, 8:00am-6:30pm
Shift: Sun-Wed, 8:00am-6:30pm

Date Added: 10-07-2021

Drug Manufacturing Technician

15194

Des Plaines, Illinois

Biotech/R&D/Science

Data Analyst

15193

Tempe, Arizona

Other Area(s)

Project Cost Control Engineer

15192

South San Francisco, California

Engineering

Description:

Project Controls Cost Engineer is delegated the responsibility for monitoring and appraising the performance of project costs and ensuring information and data is correct to ensure corrective actions are taken.

Essential Functions

1. Ensures that the Project Controls Process is carried out in accordance with the Design and Construction Engineering Manual EM Lite and the Project Controls Procedure and related Project Controls Plan.

2. Supports a Project Manager in the management of Project Controls activities of architects, engineers, contractors and other involved parties.

3. Responsible for the management of data and information within a project management system.

Responsibilities

Responsible for project cost data and supporting documentation within the Project Controls System of record, Cora
Performs reconciliation of cost data from local accounting system to Cora System
Assists the Project Manager on all levels of cost reporting and forecasting
Assists the Project Manager on all levels of negotiation and validation of Guaranteed Maximum Price contracts and change orders
Performs contract administration duties in relation to the execution and retention of project change notices (PCN)
Manage vendor PO's from creation to closeout
Reviews and validates contractual compliance of project invoices
Assists in bi-annual accrual process
Implements financial accounting training and workshops for the project management team and / or contractor
Assist Project Manager in financial project close-out
Review and support basic milestone schedule updates
Creates ad-hoc cost reports by merging data from Cora and SAP
Assists the Project Controls Manager in cost analysis exercises
Participate and lead process improvement initiatives

Experience:

5 to 10 years of experience in the area of project controls, financial control or quantity surveying

Skills:

Knowledge of:

Project Controls and Project Management Engineering and/or Business Administration Financial accounting principles

Work in Place and Accruals Skills and abilities:

Proficient in using MS-Office applications Strong analytical and high level excel skills
Ability to troubleshoot and work efficiently independently as well as within a team
Knowledge of SAP and Project Portfolio Management (eg Unifier, Cora, Ecosys, eBuilder) is preferable MS Project knowledge is a plus.

Communication and responsiveness:

Excellent verbal and written communication skills as well as strong interpersonal skills
A team player with the ability to work collaboratively and interact with employees at all levels

Education:

University degree in accounting, business administration or equivalent (e.g. cost engineer, quantity surveyor)

BEOCS

Date Added: 10-07-2021

Program Planning Controls Analyst

15191

Phoenix, Arizona

Other Area(s)

BEPC is seeking 2 talented Program Planning Controls Analysts to join our fast-growing team of consultants in Phoenix, AZ!

W2 Contract Period: 6 months with possible opportunities for extensions based on business needs and performance!

Pay Rate: $57.91/HR plus we offer Medical, Dental, Vision and Life Insurance benefits after 90 days!

Join a team of specialists that provide program analysis, process improvement, and metrics. You will partner with the Integrated program team to develop program plans, create cost and schedule baselines for large complex programs across multiple sites. You will recommend improvement actions for process and tool implementation and will interact with global program management Team, Business leaders and customers. You will coach and mentor Project Specialists with less experience to improve their skills and capabilities.

KEY RESPONSIBILITIES:

Measure program performance
Prepare and publish metrics and reports
Analyze program risk
Identify root cause, impact, and recommend corrective actions
Maintain schedule and track milestones
Lead change
Track budget and program financial data
Analyze cost schedule integration
Improve processes

REQUIREMENTS:

5+ years of Microsoft Office Project or Scheduling experience
Bachelor's degree Accounting, Business, Economics, Finance, Mathematics, or Statistics
5+ years of Project/Business Management Experience
Proficient Microsoft Office package skills e.g. Excel, Project, Outlook, PowerPoint etc.
Earned Value Management Experience

WE VALUE :

Experience with government reporting
Ability to influence at varying levels across the organization
Ability to convey subtle or complex messages clearly, as appropriate for the topic and audience
User experience of SAP system
Experience in financial data compilation, analysis and metrics management
Project Management Professional certification

BEPRO

Date Added: 10-06-2021

Research Associate I

15190

South San Francisco, California

Biotech/R&D/Science

BEPC has an open position for a Research Associate for the Biochemical and Cellular Pharmacology Department in South San Francisco, CA!

Contract W2 Period: 1 year contract with possibilities for extensions
Pay & Benefits: $39.12/hr. + Medical, Dental, Vision and Life Insurance

Description:

We have a contract position opening for a talented Research Associate to join our Biochemical and Cellular Pharmacology Department within the Research and Early Development (gRED) organization. The successful candidate will support in vitro screening & functional characterization of T cell receptors for the development of personalized neoantigen directed T cell therapies. More specifically, the individual will develop, validate and execute high-throughput cell-based assays to characterize T cell activation and cytotoxicity in vitro and support lead-finding/optimization efforts. In addition, the candidate will function as part of a multi-disciplinary project team that will coordinate with Cancer Immunology, Protein Chemistry, and Molecular Biology groups to advance personalized cellular therapies.

Who You Are

• B.S. or M.S. degree in Immunology, Biochemistry, Cell Biology, or a related field with experience in academia, biotechnology and/or pharmaceutical industry
• Practical experience in the design, development, validation and execution of biochemical and cell-based assays
• Experience with flow cytometry, cell-based functional assays, and culture of mammalian cell lines
• Ability to work independently to design, execute, and interpret experiments, and also collaborate with project teams
• Excellent teamwork, communication, time management, and organizational skills

Additional desirable skills

• A strong foundation in immunology and hands-on expertise in immune cell assays
• Experience with primary immune cell isolation and culture
• Experience with cell transfection
• Experience with Luminex assays
• Familiarity with automated or semi-automated instrumentation

BEOCS

Date Added: 10-06-2021

Acquisition Marketing Manager -Canada

15189

Newark, New Jersey

Marketing

BEPC is seeking a talented Acquisition Marketing Manager for the Canadian market to join our fast-growing team of consultants in Newark, NJ!

W2 Contract Period: 6 months with possible opportunities for extensions based on business needs and performance!

Pay Rate: $41.63/HR plus we offer Medical, Dental, Vision and Life Insurance benefits after 90 days!

About the Role:
We are looking for a results-oriented Acquisition Marketing Manager for the Canada team. You will be responsible for driving new member growth through cross-channel promotions, email, and onsite marketing. You will have direct, hands-on ownership of campaign creation, execution, and analysis, as well as cross-functional coordination with teams in Creative, Product, Marketing Operations and Technology. You will have had experience testing and elevating marketing communications through A/B testing, creative optimizations, and audience segmentation. The role requires a laser attention to detail, passion for results, commitment to action-oriented analysis, an attitude that anything is possible, and a relentless focus on the customer. The right candidate will thrive in a highly entrepreneurial, fast-changing, and collaborative environment where people are driven, enthusiastic, collaborative and not afraid to take risks. This role is based in Newark, NJ, and reports to the Acquisition Director.

Key Responsibilities:

Internal and external traffic sourcing and optimization through building strong relationships with business partners.
Own email marketing and identify new areas for growth within this communication channel
Create, update, and maintain campaigns across various internal CMS and communication tools.
Support the Acquisition team with campaign execution and managing creative and legal approval timelines.
Liaise and manage existing external affiliate partners and grow the networks of affiliates
Ensure brand consistency through design and creative updates.
Partner cross-functionally with other business team partners in Merchandising, Brand/Creative, Product, Technology, and Customer Care to deliver effective initiatives.
Proactively identify and resolve hurdles and roadblocks that may arise during campaign and project launches.
Forecast, analyze, and communicate performance results once a campaign has concluded.
Others as defined by evolving business needs for a rapidly growing online business.

Basic Qualifications:

5+ years of strong digital marketing experience driving acquisition through hands-on onsite optimizations and email campaigns.
Bachelor’s degree in Business, Marketing, Economics or a related field of study required.
Experience with web/mobile analytics tools, A/B testing tools such as Adobe Test & Target, and a content management system such as Contentful.
Ability to generate and quickly execute upon actionable recommendations based on the synthesis and analysis of data.
Experience with gathering and utilizing customer insights and turning these insights into successful marketing campaigns
Strong analytical and Excel skills.
Strong oral and written communication skills.
Self-motivated, nimble and highly results-driven in a fast-paced and deadline-driven environment.
A demonstrated record of partnering with teams (Product and UX) across the organization and influencing to achieve business results across multiple teams who may have different goals.
Strong understanding of subscription revenue business models.
Experience with both desktop and mobile platforms.

BEPRO

Date Added: 10-06-2021

Manager, Campaign Production

15187

Newark, New Jersey

Marketing

BEPC is seeking a talented Manager Campaign Production to join our fast-growing team of consultants in Newark, NJ!

W2 Contract Period: 5+ months with possible opportunities for extensions based on business needs and performance!

Pay Rate: $41.63/HR plus we offer Medical, Dental, Vision and Life Insurance benefits after 90 days!

The Marketing Operations team is looking for a sharp, enthusiastic, creative, and detail-oriented marketing professional to help meet our business objectives and create innovative customer experiences. Responsibilities include building and maintaining email templates, campaign execution across multiple channels and touchpoints, and creating and testing promotional offers. The Sr. Manager, Marketing Operations - Production will take the lead on US Outbound Marketing Campaigns and provide International support as needed. This is a critical role supporting multi-million-dollar acquisition, partnership, research, product and member engagement initiatives and ensuring streamlined and flawless planning and execution. Expertise in top tier Campaign Management tools and Email Service Providers is essential. Candidates should be email deliverability and marketing automation experts with extensive experience with HTML coding and dynamic content. The right candidate will be a quick study and demonstrate a knack for getting things done in close collaboration with technical, creative, and business teams in a fast-paced environment.

KEY RESPONSIBILITIES

Own and manage the planning and production of outbound marketing campaigns across email, push, and emerging communications platforms
Coordinate with several internal teams including acquisition, research, merchandising, Escape, Business, and Latino to consult, build, and refine their outbound marketing tactics
Develop and build sophisticated customer segments for outbound campaigns, optimizing for KPIs
Create automated marketing campaigns and migrate current manual campaigns to increase efficiency on proprietary systems
Lead QA and proofing for all outbound marketing campaigns including email, push, and automated journeys
Serve as a subject matter expert on email and push best practices and CAN-SPAM to internal clients including acquisition, research, and strategic partnerships
Integrate personalization into our outbound marketing campaigns through data providers and flexible templates

BASIC QUALIFICATIONS

Bachelor’s Degree
Minimum of 5 years’ experience in digital marketing with a focus on email and push channels
Must have hands-on production experience with building and testing emails and push notifications
Excellent understanding of CAN-SPAM
Advanced HTML skills, specifically for email design
Experience with working with campaign management tools such as Adobe, Salesforce, Unica, Marketo, Exact Target, Braze, etc.
Experience working with dynamic content services like Movable Ink
Strong organizational and communication skills, with proven ability to handle multiple projects in a fast-paced environment
Ability to speak both marketing and tech languages
Basic SQL knowledge

PREFERRED QUALIFICATIONS

Retail, ecommerce, or member engagement experience

BEPRO

Date Added: 10-06-2021

Manager, QA Production

15186

Newark, New Jersey

Marketing

BEPC is in search of a Qualified Production Manager in Newark, NJ!!

Contract W2 Period: 5 month contract with possibilities for extensions

Pay & Benefits: $41.63/hr. + Medical, Dental, Vision and Life Insurance

Job Description
The Audible Marketing Operations team is looking for a detail-obsessed outbound marketing operations manager for its marketing operations team. This person will own the QA process for email and push notification communications, from list selection to post-campaign deployment.

You will work with marketing partners, production, segmentation, and strategy teams to understand campaign requirements, then work side-by-side with the team to ensure the quality of our communications. You should have a demonstrated track record of email and push notification production, quality requirements, and test strategies. You should also be comfortable communicating with and between marketers and engineers.
Key responsibilities include:

• End-to-end QA of email and push notification campaigns including copy, links, and rendering across devices and customer types (current member, prospect, etc.)

• Ensure customer lists criteria is correct and enforce segmentation best practices

• Review journey automation and customer lifecycle campaigns to guarantee the correct customers will receive the correct message at the correct time

• Triage any issues and find quick resolutions to issues where the root cause may be an email, push, or customer segment built by the marketing operations team

• Work with customer service and IT to address escalation issues, bugs, and support requests are addressed in a timely manner

• Maintain an accurate and current QA checklist for marketing operations team members and business partners

• Test and troubleshoot email templates to ensure the rendering of static and dynamic content

• Track and submit bugs for resolution and Identify areas of opportunity that require solves to prevent recurring issues

• Manage daily/weekly progress reporting and defect resolution tracking. Report on overall QA process, findings, and insights to understand trends

• Drive efficiencies in campaign execution through QA process and improvements

• Champion the QA process to ensure high campaign production standards, define test procedures and modify to meet evolving needs

Basic Qualifications

• Minimum of 2-5 years of experience in digital marketing or production

• Expertise in managing and prioritizing multiple projects with a great attention to detail

• Bachelor's Degree in Business, Marketing, Communication, Technology Field, or related field of study

• Strong organizational and communication skills with proven ability to handle multiple projects in a fast-paced environment and ability to collaborate with cross-functional teams

• Technically capable, excellent communicator, and a desire to improve processes

• Strong analytical capability and a solid understanding of success metrics

• Proficient knowledge of MS Office

• Working knowledge and understanding of HTML

Preferred Qualifications

• Hands on experience executing emails with Salesforce/Exact Target or similar ESPs (Email Service Providers)

• Moderate to advanced HTML skills and a general understanding of email development

• Moderate to advanced experience with Project Management tools such as JIRA

• Basic SQL experience and familiarity with queries
BEOCS

Date Added: 10-06-2021

Process Development Associate

15182

San Diego, California

Other Area(s)

BEPC has a San Diego, CA area open position for Process Development Associate 1 to join our fast growing team of consultants!

Contract W2 Period: 6 month with opportunity for extensions
Pay & Benefits: $20.00/hour + Medical, Dental, Vision & Life Insurance

1st Shift M-F

Job Summary
• Responsible for the creation and transfer of manufacturing processes from R&D to Manufacturing and continuous improvement of existing processes. Also, to support commercial manufacturing needs as necessary.

Essential Duties and Responsibilities
The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.
• Maintains the Pilot Plant laboratory under cGMP conditions
• Produces development, pilot and production materials per written instructions,
• Completes ERP transactions
• Stocks and maintains the laboratory supplies
• Keeps accurate records and documentation
• Completes laboratory work and associated paperwork by assigned completion dates
• Produces notebook materials per written instructions.
• Troubleshoots manufacturing process problems.
• Develops manufacturing processes for transfer to Manufacturing.
• Assists with execution of process validation of new and existing manufacturing processes.
• Trains others on manufacturing tasks.

Physical Demands
The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
• Sit; use hands to finger, handle or feel objects, tools, or controls.
• Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl.
• Lifting/moving and carrying products weighing up to 40 pounds.
• Exposure to moving mechanical parts, vibration and/or moderate noise levels.
• Exposure to hazardous chemicals or other materials.
• Safety Shoes with Impact and Compression Protection Must be worn (will be provided).
• Exposure to blood.
• Other (please specify):

Qualifications
Education
• Bachelors degree

Experience
• 1+ years experience preferred

Skills
• Basic knowledge of QSM/GMP requirements

BEPRO

Date Added: 10-06-2021

Senior Buyer

15181

San Diego, California

Other Area(s)

BEPC has a San Diego, CA area open position for Senior Buyer to join our fast growing team of consultants!

Contract W2 Period: 12 month with opportunity for extensions
Pay & Benefits: $30.00/hour + Medical, Dental, Vision & Life Insurance

Job Duties:
100% onsite role in San Diego
Mon-Fri, normal office hours

Sr. Buyer
Manufacturing Operations

Job Summary
Responsible for purchasing commodity materials in support of Hologic's production and requirements, to include sourcing suppliers to manufacture components unique to Hologic. Exercises independent judgment to address material and supply issues. Negotiates quarterly and annual buys as required. Reviews standard and invoice purchase price variances and identifies standard pricing on an annual basis. This role is a blend of tactical and strategic activities.

Essential Duties
The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.
• Process purchase orders based upon sourcing activities for large complex suppliers
• Provide support and guidance on exceptions for transactional activities
• Support supplier onboarding
• Address supplier delivery or quality issues
• Identify and implement Best in Class processes
• Manage and lead local cross functional project teams
• Lead sourcing analysis (e.g., Spend, Business Award scenarios)
• Support and/or lead resolution of quality issues
• Responsible for supplier agreement negotiations for specific suppliers, including pricing & terms
• Monitor adherence to contract terms
• Conduct local and on-site supplier business reviews
• Participate and support the Operations Risk Management Program (ORM)
• Define and implement VIP pipeline to achieve Net 5% annual cost reduction goals
• Implement strategies and programs to achieve targeted inventory turns and implement continuous improvement projects
• Lead local sourcing and support global commodity teams
• Represent Supply Chain and/or Operations on New Product teams
• Define and provide input on Supply Chain strategy for New Product teams
• Actively supports efforts to streamline activities within the department such as the supplier Kanban process and others to be defined

Physical Demands
The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
• Sit; use hands to finger, handle or feel objects, tools, or controls.
• Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl.
• Lifting/moving and carrying products weighing up to 40 pounds.
• Exposure to moving mechanical parts, vibration and/or moderate noise levels.
• Exposure to hazardous chemicals or other materials.
• Safety Shoes with Impact and Compression Protection Must be worn.
• Exposure to blood.
• Other (please specify):

Qualifications
Education
• Bachelors degree preferred

Experience
• 3-5 years of buying procurement experience within the Medical device industry preferred
--5-10+ years of experience, we can consider a higher pay rate.

Skills
• CPIM, CPSM, CPM or PMP Preferred
• Strong communication, interpersonal, and organizational skills
• Strong working knowledge of Microsoft Office
• Knowledge of Material Requirements Planning, (i.e. Oracle)
• Accuracy, dependability and ability to work under tight requirements with minimal supervision
• Active in American Purchasing Society and American Production & Inventory Control (APICS)
• Build collaborative relationships both internally and externally

BEPRO

Date Added: 10-06-2021

Equipment Mechanic 1

15180

San Diego, California

Manufacturing

BEPC has a San Diego, CA area open position for Equipment Mechanic 1 to join our fast growing team of consultants!

Contract W2 Period: 6 month with opportunity for extensions
Pay & Benefits: $20.00/hour + Medical, Dental, Vision & Life Insurance

100% onsite role in San Diego
40 hours/week plus OT optional
Days of the week and schedule is TBD - looking for candidates w/ a flexible schedule.
Virtual interviews

Hologic is seeking an Equipment Mechanic 1 responsible for implementing and maintaining an engineering change order system including product improvements, repairs, and new product release.

Duties & Responsibilities:
• Performs scheduled and unscheduled equipment maintenance on lyophilizers, liquid fillers, labeling equipment, packaging equipment, water system equipment and filtration equipment, high speed fill equipment and flow wrapping lines
• Performs troubleshooting on electrical and mechanical systems on manufacturing equipment.
• Interacts with vendors to solve problems, determine part costs and purchase parts.
• Diagnose and repair low voltage DC and AC electrical wiring/hardware
• Maintains equipment shop tools, equipment, and organization
• Writes procedures, documents, and reports.
• Assists in development, maintenance & reporting of department metrics.
• Assists in process and quality improvement projects as assigned
• Create purchase requisitions in support of manufacturing.
• Assists in vendor and PM scheduling
• Coordinates and maintains inventory for spare parts
• Travel between various Hologic facilities for equipment maintenance
• Must be able to work weekends or other shifts on occasions.

Qualifications:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the basic knowledge, skills, and/or abilities required:
• Solid understanding in using various hand tools, multimeters, pneumatic, electrical power tools.
• Solid understanding of electrical, mechanical, and pneumatic schematics.
• Awareness of applicable mechanical, electrical and biological safety guidelines and standards.
• Ability to diagnose mechanical, electrical, and pneumatic equipment problems.
• Knowledge of windows-based computer systems.
• Knowledge of microprocessor and automation controls.
• Must have reliable vehicle and valid drivers license to support multiple facilities
• Ability to operate mills, lathes, drill press, and power saws for fabrication of machine parts
• Detailed oriented with strong verbal and written communication
• Ability to articulate information to coworkers and vendors
• Ability to lift 50 lbs.
• Experience in a GMP environment preferred

Education and Experience:
• Requires high school diploma or GED, trade school, or Military and 2 - 4 years related experience or AA and 0-2 years related experience
• Experience with calibration/engineering programs and electronic document management systems preferred.
• Must have good written and verbal communication skills
• Basic knowledge of Microsoft Office programs, i.e., Word, Excel
• Basic knowledge of QSR & ISO requirements
• Ability to multi-task and operate effectively in a fast paced environment
• Experience with inventory management system is preferred but not required

BEPRO

Date Added: 10-06-2021

User Support Technician

15179

Marlborough, Massachusetts

IT/Networking/Hardware

Summary of Duties and Responsibilities
• IS Help Desk support (On rotating basis with some after-hours coverage)
o Answer help desk phone calls
o Route help desk tickets to appropriate technicians or support groups
o Provide on the spot troubleshooting as time allows
o Provide support through online chat system
o Provide walk up support
• Provide local support for the following systems (installation, upgrades, troubleshooting):
o PC/Laptop Hardware and Software
o Network Peripherals, Printers, Copiers
o Telephone System
o Enterprise/Business Applications
• Maintain loaner laptops and projectors
• Hardware procurement, inventory, disposal support

Qualifications
To perform this job successfully, an individual must be able to perform essential duties satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to do the essential functions.
• Windows 7 & 10 experience
• Microsoft Office 2013 experience or above
• Knowledge of Laptop/Printer Hardware
• Networking and Wireless skills a plus
• PC/Laptop build experience
• Active Directory and Windows server product experience desired
• Desktop support tools knowledge
o Anti-Virus, Malware, Spam experience desired
• Ability to triage, troubleshoot, and resolve basic PC/Network problems quickly and accurately; contacts vendors as needed
• Ability to be an active participant and contributor on a professional IS Support Team
• Good communication skills, telephone support skills, and interpersonal skills with a customer service focus
• Ability to plan/organize time and workload
• Ability to follow standard process/procedures
• IT service management system experience desired (ServiceNow experience a plus)
• Ability to work assignments that are routine in nature and recognize deviation from accepted practice

Education
• BA/BS MIS or CIS (or related technical discipline) desired

Experience
• 0-1 years experience in IS Help Desk support

Specialized Knowledge
• Good troubleshooting and technical skills
• Good communications skills
Additional Details (Including Physical & Mental requirements)
• Must be able to lift 50 lbs.

BEOCS

Date Added: 10-06-2021

Marketing Reviewer

15178

New Jersey, New Jersey

Professional

BEPC is seeking a dynamic Content Marketing Project Manager to join our fast-growing team of consultants!

W2 Contract Period: 5 months with possible opportunities for extensions based on business needs and performance!

Pay Rate: $40.74/HR plus we offer Medical, Dental, Vision and Life Insurance benefits after 90 days!

Responsibilities include but are not limited to:

Create a project plan that properly prioritizes and clearly maps multiple product videos that need to be updated and created.
Meet with agencies to get accurate quotes for external design and video update support.
Work with SMEs and product owners to make sure all updates are made and applied correctly.
Ensure all content meets GBT’s Tone of Voice and Editorial standards.
Ensure all content is being held to correct deadlines and if deadlines cannot be met, communicate with appropriate stakeholders to redefine expectations.
Work directly with brand team to ensure final content pieces are compliant with GBTs external content standards.
Proactively apply brand, legal, and compliance rules across materials for a streamlined review process of external content pieces.

Skills:

Extremely organized, strong project manager.
Experience working within strict project plans and deadlines.
Experience working within strict brand guidelines
Experience working cross-functionally within a large organization.
Can prioritize content pieces appropriately across multiple documents.
Experience in copywriting and editing.

Qualifications:

3+ years’ experience project management
1+ year’s experience in content marketing
1+ year’s experience in copywriting/copyediting
Strong project management and organizational skills as well as extreme attention to detail

Programs:

Adobe Photoshop, Premier, InDesign, Marketo, Workfront, Microsoft Word, PowerPoint, Excel

Nice to Have:

Experience with technology company
Experience in B2BExperience with project management tools
Bachelor’s degree in English, Communications, Business

BEPRO

Date Added: 10-05-2021

Senior Director, Publisher Relationships

15175

Newark, New Jersey

Professional

BEPC is seeking a talented Senior Director, Publisher Relationships to join our fast-growing team of consultants in Newark, NJ!

W2 Contract Period: 6 months with possible opportunities for extensions based on business needs and performance!

Pay Rate: $74.66/HR plus we offer Medical, Dental, Vision and Life Insurance benefits!

As the Senior Director, Publisher Relationships, you will oversee all strategy related to releases and promotions from partner providers rooted in publishing, education, and entertainment.

This role strategically leads and oversees our largest partnerships, including content creation, client management, marketing and promotion, and amplifying the brand. The right candidate will utilize deep content knowledge and partnerships experience to influence and maintain our relationships with publishing partners by guiding advantageous business decisions, leading a team and undertaking creative solution finding.

KEY RESPONSIBILITIES

Oversee content releases from all key providers, ensuring that we are driving sales and listening of these top priorities through creative marketing, strong internal collaboration, and solid external partnership management.
Oversee partnerships with large publishing partners ensuring marketing initiatives gain support both internally and externally to feature content in marketing campaigns across and author platforms.
Serve as the go-to expert on all high-touch partnerships, both internally and externally and identifying opportunities for further growth for all parties.
Attend all quarterly business reviews and partner updates to ensure we are achieving goals and growth as a result of these partnerships.
Work closely with the Business Affairs team to align on goals for partnerships, find efficiencies, and resolve any issues.
Ensure there is cohesion across the organization when it comes to partner content development internationally.
Manage a manager and oversee management of an Associate Manager and Publisher Relations Specialist
Special projects as assigned by the Vice President US Publisher Relations and Sr. Director of Content Marketing to facilitate the team’s smooth operation.
Lead the content partnership with high-profile external brands, working closely with Editorial, Business Affairs and Marketing on the creation, distribution, and promotion of all projects.
Where applicable, serve as key member of special assignment teams, where key responsibilities could include: establishing business and operational plans, identifying, recruiting, and managing talent in the content space, partnership with the product team for any tech enhancements required
Responsible for all 3^rd party external partner management in a promotional capacity, including any new partnerships signed by CA&D, including but not limited to Wondery, Pushkin, and smaller independent publishers. It will be critical to manage these partners throughout our new service launches, using considerable creativity and foresight.

In addition, the responsibilities of the Program Director, Podcast Development Program, is a part of this role. In this particular segment of the position, the role will oversee all areas of the program, ensuring any challenges are solved and creators are successfully supported by the production team through the development process. Additionally, this role will:

Have financial accountability over budget and scope of project.
Manage Emerging Voices Advisory Board relationships and talent to ensure all obligations are fulfilled.
Special projects: Working with our impact groups and beyond to create pathways to connect with diverse creators to ensure our creators represent the human spectrum and further amplify the program’s imperatives.

BASIC QUALIFICATIONS

Bachelor’s Degree required
10+ years of experience in related fields (entertainment, media or publishing)
Outstanding written and verbal communication skills
Expertise in client management
Detail-oriented and a strong decision maker
Comfortable with high-volume throughput
Thrive in a high-energy, high-intensity and rapidly evolving environment
Highly collaborative with teams and individuals across the institution

PREFERRED QUALIFICATIONS

Experience from networks, studios, publishers or tech giants/startups
Talent management
Both data-driven and creative
Marketing or PR experience
A love of audio entertainment

BEPRO

Date Added: 10-05-2021

Manufacturing Technician 1 (2nd Shift)

15174

Londonderry, New Hampshire

Manufacturing

Operator I

15171

Temecula, California

Manufacturing

Senior Advanced Mechanical Engineer

15170

Muncie, Indiana

Engineering

CAD Designer

15169

Muncie, Indiana

Other Area(s)

Trainer

15168

Westbrook, Maine

Management

BEPC has a Westbrook, ME area open position for a Trainer to join our fast growing team of consultants!

Contract W2 Period: 4 months with opportunity for extensions
Pay & Benefits: $27.60/hour + Medical, Dental, Vision & Life Insurance

Work Shift: 1^st Shift, 11:30am to 10pm EST

Technical Degree or the equivalent combination of education and experience

Provide assistance in designing and implementing training evaluation measurement tools, perform training evaluation and needs assessment.

DETAILS:

This position is NonExempt.
Hours over 40 will be paid at Time and a Half.
Work with Training effectiveness team and review board.
Create training test and task assessments and identify specific skills areas or competencies for job functions.
Perform data reduction and analysis, create graphs and prepare metrics.
Education requirements: 4 year degree.
Skills/experience requirements: Instructional design and training experience.
Ability to perform training evaluations & needs assessments and utilize data to develop effectiveness measurements.
Ability to develop skills implementation & performance feedback mechanisms.
On the job training (OJT) assessment and evaluation skills.
Human resource development skills and scholastic application experience.
Project management skills.
Very good computer skills and proficiency at using Microsoft Word, Excel spreadsheets and Power Point programs.
Ability to reduce data and create presentations with data and other graphical representations.
Excellent communication skills with all levels of employees.
Adaptable.
Excellent interpersonal and teamwork skills.
Physical requirements: Sit for 9 hours, use a computer terminal 9 hours per shift. Walk, work alone, and work with others.

BEPRO

Date Added: 10-05-2021

Operator I - 2nd Shift

15167

Irving, Texas

Manufacturing

Pay Rate: $16.32

This position is responsible for the production of high quality medical devices within a manufacturing cell. Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies. Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed. Ensure that relevant job documentation for cell operations and functions is accurate and up to date. Be able to clearly communicate ideas, problems and solutions to all levels of manufacturing management in both written and oral form. Maintain a positive attitude when interacting with internal customers and external customers such as tours. Follow safety guidelines and utilize appropriate safety devices when performing all operations. Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics. Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products. Demonstrates a basis understanding of Lean Manufacturing. Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations. Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions - Understanding of and ability to utilize electronic data collection systems and computer software packages. Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance. Ability to handle and maneuver small components and parts. Ability to make critical decisions and judgments with minimal supervision.

High school degree or equivalent preferred.

BEOCS

Date Added: 10-05-2021

Test Technician

15166

Irving, Texas

Manufacturing

BEPC is seeking 10 talented Test Technicians to join our fast-growing team of consultants in Irving, TX!

W2 Contract Period: 6 months with possible opportunities based on business needs and performance!

Pay Rate: $20.83/HR plus we offer Medical, Dental, Vision and Life Insurance benefits!

Job Summary:

Working under general supervision, this position is responsible for the production of high-quality medical device instruments. This position includes detailed assembly and testing of various electronic components and finished devices in a controlled manufacturing environment.

Job Responsibilities:

Performs testing of electronic components and assemblies using automated test equipment
May perform mechanical assembly of electromechanical subassemblies and devices
Ability to read, comprehend and follow written procedures; understand and follow verbal instructions. May instruct others in the use of all manuals, test procedures and documentation associated with specialized equipment.
Reads and interprets engineering drawings, schematics and complex test procedures.
Participates in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.
Maintains accurate records to ensure Device History Records and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Prioritizes work by determining the sequencing and timing of different jobs based on precedence and importance.
Positively represents the company during tours by demonstrating techniques and sharing appropriate information.
Supports all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
Complies with U.S. Food and Drug Administration (FDA) regulations, ISO or other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
Adheres to all environmental, health and safety SOP’s, equipment, policies and procedures, including any department specific requirements.
Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Minimum Qualifications:

Experience with electronic assembly and test in a medical device industry preferred.
High School Diploma or equivalency is required
2 or more years experience with electromechanical assemblies/electronic manufacturing, technical certifications, etc. preferred

Preferred Qualifications:

Experience in troubleshooting equipment, building and or testing of electronic assemblies
Working knowledge of IPC standards and use of complex tools and equipment specific to functional areas
Experience in GMP, ISO, and FDA controlled environments preferred
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
Multitasks, prioritizes and meets deadlines in timely manner.
Strong organizational and follow-up skills, as well as attention to detail.
Ability to maintain regular and predictable attendance.
Ability to work scheduled overtime as required is preferred.
Ability to hand and lift up to 25 lbs. as needed for specific job functions ? Must be able to sit and/or stand for long periods of time.
Ability to frequently sit, stand, walk, reach within hands and arm’s length, stoop, kneel and crouch.

BEOCS

Date Added: 10-05-2021

Operator I

15165

Temecula, California

Manufacturing

Lead System Engineer

15164

Phoenix, Arizona

Engineering

Experienced Control Systems engineer
Key Responsibilities
• Requirements analysis
• Requirements decomposition
• Systems design
• Systems integration
• Systems validation & verification
• Customer interaction
• Project oversight

experience using Doors
sound understanding of req allocation for Hardware and Software

Bachelors in Electrical/Mechanical/Systems/Aerospace degree.
5+ years experience and prefer 8+
Other Degrees can be acceptable if they have over 10 years of related experience.
Familiarity with Engine Controls, Requirement Traceability, Team Center, and Doors.

- Beneficial FAR 33 knowledge
- Experience drafting, submitting and approval of FAA Plans/Procedures/reports
- Experience with both Electrical, Mechanical, and fluid engine components
- Beneficial to have knowledge of Honeywell Engine products like (TPE331, TFE731, HTF7K, T55, F124)

Key Responsibilities
• requirements analysis • requirements decomposition • systems design • model based development system design • systems integration • systems validation & verification • Part analysis and supplier Transition experience

Responsible for the support of the sales representatives by providing technical knowledge to clients and potential clients.
Provides support in both pre- and post-sale by attending presentations, product demonstrations, and installations/implementations.
May require a bachelor's degree and at least 6-8 years of experience in the field or in a related area.
Familiar with a variety of the field's concepts, practices, and procedures.
Relies on extensive experience and judgment to plan and accomplish goals.
Performs a variety of tasks.
May lead and direct the work of others.
A wide degree of creativity and latitude is expected.
Typically reports to a manager or head of a unit/department.

BEOCS

Date Added: 10-05-2021

Lead Software Engineer

15163

Phoenix, Arizona

Engineering

Key Responsibilities
• Requirements analysis
• Requirements decomposition
• Systems modeling and design
• Model based development system design
• Systems integration
• Systems validation & verification
• Customer interaction

YOU MUST HAVE
• Bachelors degree in Engineering

WE VALUE
• 7+ years of experience in control systems engineering
• Knowledge of the systems development lifecycle
• Understanding of gas turbine engines and control systems
• Knowledge of Matlab/Simulink
• Individuals that quickly analyze, incorporate and apply new information and concepts.
• Diverse and global teaming and collaboration
• Effective communicator
• Individuals who are self-motivated and able to work with little supervision, who consistently take the initiative to get things done.
• Ability to adapt dictated by project changes
• Multi-tasking and has the ability to manage a variety of complicated tasks.

Designs, modifies, develops, writes and implements software programming applications.
Supports and/or installs software applications/operating systems.
Participates in the testing process through test review and analysis, test witnessing and certification of software.
Designs, plans, and coordinates work teams.
Provides technical support to project team members.
Requires a bachelor's degree in a related area and 6-8 years of experience in the field.
Familiar with a variety of the field's concepts, practices, and procedures.
Relies on experience and judgment to plan and accomplish goals.
Performs a variety of tasks.
Leads and directs the work of others.
A wide degree of creativity and latitude is expected.
Typically reports to a head of a unit/department.

BEOCS

Date Added: 10-05-2021

Engineer, Research & Development

15160

Atlanta, Georgia

Engineering

Operator III

15158

Temecula, California

Manufacturing

BEPC INC IS LOOKING FOR MEDICAL DEVICE ASSEMBLER III IN TEMECULA CALIFORNIA!

W2 CONTRACT: 2 years with extension or permanency possibilities.

PAY: $18.26/hr + Medical dental vision and life insurance.

HOURS: 10 am to 6:30 pm (M-F)

JOB DESCRIPTION:

DUTIES MAY INCLUDE:

Electronic assembly, casting/coating functions, mechanical assembly and packaging.
Cleans tools and equipment per documented procedures. Disposes hazardous waste material on corresponding hazardous waste areas.
Assembles medical devices and related components.
Depending on work area, it may be a controlled cleanroom environment.
Use of microscopes, use of hand tools, razor blades, syringes, soldering, adhesive bonding, and operating various equipment.
Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed.
Performs visual inspection and precision measurements on components and assemblies.
Performs tests on units using computerized test equipment. Repairs and corrects devices/components using microscopes and applicable tools.
Packages devices ensuring all parts are accurate and documentation is complete.
Maintains accurate records to ensure travelers, shop floor paperwork and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Follows safety guidelines and utilize appropriate safety devices and equipment when performing all operations.
Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics.
Notifies supervisor or lead of the need to replenish supplies/materials and of any production difficulties that cannot be readily corrected.
Participates with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Cooperates in keeping a clean, sanitary work environment throughout the building.
Performs other related duties as directed or assigned.

REQUIREMENTS:

Must be able to read, comprehend and follow English written procedures at a 6th grade level.
Must have good basic math skills at a 6th grade level.
Must be able to speak, follow verbal instructions and communicate effectively in English.
Possesses understanding of and ability to utilize electronic data collection systems and computer software packages.
Must have good dexterity to handle and maneuver small components and parts.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to make critical decisions and judgments with minimal supervision.

EDUCATION: High school diploma required 5+ years of experience.

BEOCS

Date Added: 10-05-2021

Operator II

15157

Temecula, California

Manufacturing

BEPC INC IS LOOKING FOR MEDICAL DEVICE ASSEMBLER II IN TEMECULA CALIFORNIA!

W2 CONTRACT: 2 years with extension or permanency possibilities.

PAY: $18.00/hr + Medical dental vision and life insurance.

HOURS: 10 am to 6:30 pm (M-F)

JOB DESCRIPTION:

DUTIES MAY INCLUDE:

Electronic assembly, casting/coating functions, mechanical assembly and packaging.
Cleans tools and equipment per documented procedures. Disposes hazardous waste material on corresponding hazardous waste areas.
Assembles medical devices and related components.
Depending on work area, it may be a controlled cleanroom environment.
Use of microscopes, use of hand tools, razor blades, syringes, soldering, adhesive bonding, and operating various equipment.
Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed.
Performs visual inspection and precision measurements on components and assemblies.
Performs tests on units using computerized test equipment. Repairs and corrects devices/components using microscopes and applicable tools.
Packages devices ensuring all parts are accurate and documentation is complete.
Maintains accurate records to ensure travelers, shop floor paperwork and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Follows safety guidelines and utilize appropriate safety devices and equipment when performing all operations.
Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics.
Notifies supervisor or lead of the need to replenish supplies/materials and of any production difficulties that cannot be readily corrected.
Participates with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Cooperates in keeping a clean, sanitary work environment throughout the building.
Performs other related duties as directed or assigned.

REQUIREMENTS:

Must be able to read, comprehend and follow English written procedures at a 6th grade level.
Must have good basic math skills at a 6th grade level.
Must be able to speak, follow verbal instructions and communicate effectively in English.
Possesses understanding of and ability to utilize electronic data collection systems and computer software packages.
Must have good dexterity to handle and maneuver small components and parts.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to make critical decisions and judgments with minimal supervision.

EDUCATION: High school diploma required2+ years of experience.

BEOCS

Date Added: 10-05-2021

Operator I - 2nd Shift

15155

Menlo Park, California

Manufacturing

W2 contract period 11 months
Pay Rate: $22 Hourly

This position is responsible for the production of high-quality medical devices within a manufacturing cell.

Details

Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.
Be able to use tools such as screwdrivers, tweezers, and microscopes.
Performs routine assignments according to specified and/or standardized procedures.
Work is closely and continually reviewed.
Ensure that relevant job documentation for cell operations and functions is accurate and up to date.
Be able to clearly communicate ideas, problems and solutions to all levels of manufacturing management in both written and oral form.
Maintain a positive attitude when interacting with internal customers and external customers such as tours.
Follow safety guidelines and utilize appropriate safety devices when performing all operations.
Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.
Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
Demonstrates a basis understanding of Lean Manufacturing.
Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions.
Understanding of and ability to utilize electronic data collection systems and computer software packages.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to handle and maneuver small components and parts.
Ability to make critical decisions and judgments with minimal supervision.
High school degree or equivalent preferred.

Date Added: 10-05-2021

Manufacturing Engineer II

15153

Menlo Park, California

Engineering

Product Technician

15151

Sturgis, Michigan

Manufacturing

Product Technician

15148

Sturgis, Michigan

Manufacturing

Product Technician

15147

Sturgis, Michigan

Manufacturing

Forklift Driver I - 3rd Shift

15146

Sturgis, Michigan

Manufacturing

Production Worker I - 3rd Shift

15145

Sturgis, Michigan

Manufacturing

Forklift Driver I - 2nd Shift

15144

Sturgis, Michigan

Manufacturing

Forklift Driver I - 2nd Shift

15143

Sturgis, Michigan

Manufacturing

Production Worker I - 2nd Shift

15142

Sturgis, Michigan

Manufacturing

Processing Operator I - 3rd Shift

15141

Sturgis, Michigan

Manufacturing

Manufacturing Engineer

15135

San Diego, California

Engineering

BEPC Inc. is searching for a Manufacturing Engineer in San Diego, CA.

W2 CONTRACT: 3 – month contract with possibilities for extensions.

PAY AND BENEFITS: $42.00 / hr. + Medical, Dental, Vision and Life Insurance.

SCHEDULE: MON. – FRI. 8A.M. – 5 P.M.

Job description:
The Manufacturing Engineer is responsible for providing engineering support services including evaluation, purchase, installation, and qualification of new manufacturing equipment.
Responsibilities:
• Provides general engineering services and support
• Manage the design, acquisition, installation and commission of mechanical/electrical equipment, systems and parts to support manufacturing
• Perform process transfers from Engineering to Manufacturing including processes and equipment training
• Provides technical engineering support for repairing, troubleshooting and modifying equipment and systems
• Supports equipment mechanics
• Create and/or modifies equipment maintenance procedures
• Manage outside vendor’s with installation, qualification and sustaining support of equipment and processes
• Writing and reviewing operating procedures, documents and reports
• Performs equipment, process and product performance testing
• Manage qualifying and changes in raw materials, vendors and perform investigations for non-conformance events
• Provides QS validation input and support for new equipment and process validations
• Writing and executing Installation, Operation, and Performance Qualification Validations; including writing final reports
• Reviews and approves calibration datasheets
• Process Qualifications, Design control methods, working knowledge of microprocessor controls, utility distribution systems and process engineering
• Knowledge of manufacturing automation systems and best design practice
• Knowledge of CGMPs, ISO 13485 and FDA 21 CFR 820
• Working knowledge of Windows based programs
• SolidWorks or Pro/E (3D modeling knowledge)
• Minitab or equivalent statistical software
• Sit; use hands to finger, handle or feel objects, tools, or controls.
• Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl.
• Lifting/moving and carrying products weighing up to 40 pounds.
• Exposure to moving mechanical parts, vibration and/or moderate noise levels.
• Exposure to hazardous chemicals or other materials.
• Exposure to blood.
Education and Experience:
• BA or BS degree
• 3-9 years of related industry experience

BEOCS

Date Added: 10-05-2021

Trade Ops Coordinator

15133

East Hanover, New Jersey

Professional

BEPC Inc is looking for a Trade Ops Coordinator in East Hanover, NJ!
Contract W2 Period: 1 year contract with possibilities for extensions
Pay & Benefits: $24.82/hr. +Medical, Dental, Vision and Life Insurance

This position sits remote but candidate must work East Coast hours. Your responsibilities include, but are not limited to: Responsible for daily data submission from customers, ensuring all feeds are complete and communicate areas for improvement with customer Primary point of contact for 3PL (Third Party Logistics Companies) Responsible for the analysis and resolution of all Return Authorization issues as it relates to customer or product. Also, relating to the customer or product once product is returned to the warehouse (3PL Queue). Work with Warehouse manager and returns team on issues regarding product returned back with missing RA data elements Order processing – ensures accurate and timely processing of all orders in SAP. Maintenance and validation for updating Indirect Customer Master Data is required. Utilizes CRM (Salesforce.com) to retrieve workload and document all customer channel communications Participate in special projects and ad hoc reporting Responsible for adhering to all company, and departmental policies and procedure Multi-channel Contact Center coverage during standard business hours. Creates statistical reports relating to returns to be sent weekly to direct trading partners as well as Third Party Logistics Companies. Responsible for accurate and timely completion of HDA and Product Set up documentation in preparation for new product launches.
Skills:	Minimum of 2 years of experience in operations, sales and distribution or customer support. Effective interpersonal and organizational skills Good problem solving, decision making, verbal and written skills. Ability and desire to work both independently and within a team coupled with a sense of urgency Flexibility and desire to interact with both internal and external customers. Proficiency in computers is needed for this role. MS Excel (Intermediate to advanced skills), Word, and PowerPoint.
Education:	Bachelor’s Degree is required for this position Will consider graduate students who are able to work full time. Desirable Requirements: Experience with Salesforce.com or other CRM System SAP system experience

BEOCS

Date Added: 10-05-2021

Project Manager II

15131

East Hanover, New Jersey

Project Management

BEPC has an East Havoner NJ area open position for Remote PMP to join our fast-growing team of consultants!

Contract W2 Period: 1 YEAR with possibilities for extension
Pay & Benefits: pay/hr based on experience + Medical, Dental, Vision & Life Insurance
Must live in EST time zone

KEY RESPONSIBILITIES
Provide project management support for a US-based Health Economics & Outcomes Research (HEOR) Function including its RWE & Data Science team to specifically implement a systematic agile system and information management process that is used to track project management activities, resources, deliverables and timeline for research projects or analytic products across multiple therapeutic areas (TA) or disease areas; specific tasks may include but not limited to:

Liaise with each TA research or Pod Team including researchers, data engineers and data scientists on a regular basis to create, plan, assign, update and track progress of projects and specific tasks within project using a project management tool/system Participate in, document meeting minutes and assist with scheduling of team's meetings Act as the point of contact and communicate project status to each TA research or Pod Team Identify, propose, and implement new processes, workflows, and technology to constantly improve project efficiency

Provide periodic progress summary and updates to the Executive Director of RWE & Data Science or other stakeholders to eliminate barriers and to ensure work efficiency Create and maintain comprehensive project documentation, plans and reports/dashboard or internal communications, as needed Ensure consistent standards and requirements are applied across projects Implement a philosophy of continuous process improvement ('Kaizen')

SKILLS:
Experience in project management, from conception to final deliverable, with direct work experience as a Project Manager or similar role preferred Solid organizational and planning skills, including multitasking and time-management.
Attention to detail Strong interpersonal and teamwork skill.
Experience with using Agile project management tool/system, preferred Pharma background, preferred PMP certification- REQUIRED!!!
Scrum Master - PREFERRED!
Manager is open to remote workers in the US, preferably EST time zone.

EDUCATION:

PMP certification required; Bachelor's degree

https://www.ziprecruiter.com/job/4ca57140

BEOCS

Date Added: 10-04-2021

Research Associate

15130

South San Francisco, California

Biotech/R&D/Science

Production Support Document Specialist

15128

Wilson, North Carolina

Manufacturing

BEPC has an open position for a Production Support Document Specialist in Wilson, NC!

Contract W2 Period: 1 Year contract with possibilities for extensions
Pay & Benefits: $20/hr. + Medical, Dental, Vision and Life Insurance

Partners with quality assurance, quality control, operations, engineering, maintenance, calibration, safety and supplier quality management to ensure appropriate and timely completion of SOPs periodic review and applicable updates of SOPs and Forms.
Be the owner of CAPAs and generate Protocols for execution of different activities required by deviations or special need of the operations area.
Interacts will all levels of staff and provides status updates as well as present the strategy for approval of documents
Determine appropriate corrective actions and preventative actions (CAPAs) to prevent reoccurrence of the deviation with realistic timelines for completion.
Author SOPs, Forms, Protocols and other GMP documents to support investigations, periodic reviews, projects or CAPA plans.
Own and complete Corrective and Preventive actions and will be responsible to drive on time closure of such actions.
Set up and run meetings with cross functional teams.
Work with minimal supervision to drive SOPS, forms, protocols, etc to closure.
Work with the Manufacturing Science & Technology, Engineering, Subject Matter Experts and Quality Approvers to complete revision or updates on SOPs, Forms, Protocols and other documents.
Illustrate strong communication, project management and leadership skills, including the ability to interact and influence others at various levels of the organization.
Performs other duties as assigned in support of the operations area.
Adheres to all applicable procedures, cGMPs, company policies and any other quality or regulatory requirements. (For example: OSHA, DEA, FDA, EMEA, ANVISA, HS&E, etc.)

Skills:

2-3 years experience with BA degree.
5 years of manufacturing experience with an Associates degree or a minimum of 10 years manufacturing experience and equivalent in related area.
Experience in a regulated environment such as medical devices, pharmaceuticals or biotech industry.
Must have a thorough understanding of the pharmaceutical/biotech manufacturing process and equipment, preferably solid oral dosage, and current Good Manufacturing Practices (cGMPs).
Must have good analysis, troubleshooting, and investigation skills.
Fluent in written and spoken English

Skills and Experience:

CGMPS
FDA
MANUFACTURING PROCESS
MEDICAL DEVICES
OPERATIONS
Additional Skills:
PHARMACEUTICAL/BIOTECH
CALIBRATION
CAPA
CORRECTIVE AND PREVENTIVE ACTION
GMP
LEADERSHIP SKILLS
MAINTENANCE
PROJECT MANAGEMENT
QUALITY ASSURANCE
QUALITY CONTROL
SOPS
SUPPLIER QUALITY

BEOCS

Date Added: 10-01-2021

Global OCE Marketing Manager

15127

East Hanover, New Jersey

Management/Operations

BEPC Inc is looking for a Global OCE Marketing Manager in East Hanover, NJ!
Contract W2 Period: 5 months contract with possibilities for extensions
Pay & Benefits: $50.00/hr. +Medical, Dental, Vision and Life Insurance

**THIS POSITION WILL BE 100% REMOTE AT THIS TIME, Need candidates local to East Hanover**

Duties:
Support OCE Director with Omni-Channel campaign engagement strategies, which will integrate across customers and channels, focusing on improved customer experiences as well as patients. Responsible for day-to-day campaign management and strategic execution of the Omnichannel activities and tactics to ensure that objectives and expectations are consistently met or exceeded among several agencies and internal partners.

This position will support a specific brands and indications - leveraging and orchestrating Omni-Channel marketing campaigns and digital solutions.
This position will also facilitate content management for our priority brands ensuring that digital content is created in line with the priority brand needs and to satisfy the requirements of our field force and our target audience across all channels and platforms and disseminated to our regions and countries.

Operate, Track, Report and Improve:

Key liaison between Omnichannel strategists, External agency partners, PLS, IT and Commercial Track and Maintain overall project timelines.
Follow up teams and ensure the project Milestones are delivered as scheduled Support with IT Documentation and responsible for process control during asset development.
Work with IT to complete/review IT Docs, get brand team signatures.
Review and confirm URS document
Work with IT/PLS/ and external creative agencies to ensure assets delivered are according to the NVS standards.
Ensure Assets are verified per department's best practices.
Schedules meetings with external agencies and IT/PLS to clarify requirements for websites and media asset delivery
Responsible for UAT and quality control of the Multichannel assets Ensure the assets developed are in line with business requirements
Track and Communicate status/risks to Multichannel strategists and Key stakeholders regarding digital assets
Ensure that the PROGRES (MLR) changes and/or edits are incorporated by the agency of record Work with PLS and External agencies to ensure all Global assets are archived in corresponding platforms like Reel Deal and to support countries with localization Continual assessment and process improvements.
Proactively identifies opportunities for process improvement and works closely with the appropriate stakeholders to execute changes where most appropriate
Provide support to countries in order to facilitate local adaptation of globally created digital assets as well as with Launch Planning and Financial Management: supporting the annual MCM brand Budget Planning Process, encouraging focus on Promotional Effectiveness, Customer Journey mapping and Innovation.

Skills:

Initiate vendor evaluation, proposals, TO, contract, and kick-off. This includes:
vendor management, detailed activity tracking, updates & timeline management with a focus on efficiency of delivery and reporting.
Develop campaign strategies for brands, both global and local and deliver end to end execution of said plans.
Full responsibility for content dissemination to create efficiencies in our content creation across brands. Uploading of content to the various digital asset management platforms and portals.
Execution of campaigns, timeline management, vendor management, reporting on campaign performance, utilization analysis of content, content dissemination, sharing of best practice, dedicated to a specific priority brand.
Responsible for timely campaign performance and metrics in order to ensure that promotional plans are being executed as planned and providing optimal impact.

Channel Mix Responsibilities:

Develop strong, competitive intelligence across channels to stay abreast of best-in-class experiences and develop appropriate strategic and tactical responses in the market.
Assesses operational performance, determines best practices and facilitates continuous process improvement to maximize efficiency.
Evaluates, aligns and combines channels to reinforce each other, maintain a consistent experience, and deliver consistent value to users. production and re-utilization of Content.
Develops content requirements, including structured content and adaptive content recommendations
Assist in the creation of annual digital plans, which may include: strategy, tactics, timing, and budget Participate and organize concept kickoffs for new digital projects.
Share learnings with extended team (OCE Team, Brands, countries, etc.)
Maintain a strong working relationship with best in class agencies
Measure impact to results with qualitative & quantitative measures Help assess, develop & deliver innovative engagement solutions
Develop and disseminate high volumes of targeted and relevant content.

Education:

Bachelor's required.
English (Oral and Written)
5+ years of proven experience managing delivery of and/or digital
5+ projects and services across complex matrix environments
3+ years of digital Pharma and/or agency experience
Understanding of regulatory environment preferred Creative problem solver who is good a solving complex problem in a matrix organization
Demonstrated business acumen, ability to consult internally and/or externally
Proven ability to manage multiple projects and managers
Be accountable for individual results
Demonstrated strong skills in oral/ written communication, project management experience in digital operations considered a plus
Strong skills in effective service leadership, project pipeline, budget control, delivery management and reporting, risk and issue analysis and quality assurance.
With this in mind, an understanding of the principles of project management methodologies and processes is vital

BEOCS

Date Added: 10-01-2021

CW Credit Investigator

15126

Chandler, Arizona

Administrative

Project / Training Coordinator

15124

Cornelia, Georgia

Professional

Summary:

The Training Specialist leads the site training function to develop and implement training programs that support company objectives and meet regulations.

Directs staff in the design and administration of training programs to train all levels of personnel. Develops programs and practices to identify developmental needs and monitor trends. Prepares personnel to increase effectiveness in present assignments and assume more responsibilities.

ESSENTIAL FUNCTIONS/DUTIES and RESPONSIBILITIES:

Responsibilities may include, but are not limited to:

Consults with management, employees, and departments to identify training needs, address them and achieve the end result of effective training solutions.
Recommends the creation or acquisition and delivery of training programs that meet the company's needs.
Implements training metrics to monitor training effectiveness against needs of the business.
Summarizes training program assessment data and participant attendance reports and submits or presents to management.
Supervises, coaches and develops assigned personnel.
Ensures that all assigned personnel have the education, training and experience, or a combination of these, in order to carry out all job duties and responsibilities.
Creates new training materials as required in collaboration with subject matter experts.
Communicates and escalates issues to the next management level as needed
Develops and maintains a training program to support the company needs and meet applicable local, federal and state laws/regulations.
As applicable is responsible for the site implementation of TWI (Training within Industry) methodology and others directed towards optimizing training practices across all operational areas.
Experience as subject matter trainer to conduct training sessions i.e. quality system related topics and to certify employees as trainers across the company.
Knowledge in Learning Management System (LMS) and its use to deploy training programs and requirements across the company.
Application of Basic Project Management and/or Process Excellence knowledge and skills
Reviews, interprets and explains documents such as technical data, safety rules, operating and maintenance instructions, and procedure manuals.
Performs any other task as required by Training Leaders & Managers
Leads projects of low / Medium / High complexity.
Create procedures and / or collaborate in relation to the training processes (administration of training curricula, training registers, training within an industry, OP Cert, archive, external regulatory agencies, operator certification, audit processes etc.)
Experience with managing projects
Good understanding of quality training
Performing needs assessments and curricula design a plus
Good communication skills with customers

EDUCATION and/or EXPERIENCE:

A minimum of a Bachelors Degree is required in Business, Education, Industrial Engineering or other related technical field.
A minimum of 1 year of relevant work experience is required, with at least 1 year working in a training capacity / A minimum of 2 years of relevant work experience is required, with at least 2 years working in a training capacity. / A minimum of 4 years of relevant work experience is required, with at least 2 years working in a training capacity

A minimum of 1 year / 2 years / 3 years of projects management experience is required.
Experience designing and presenting successful training programs required.
Experience working in manufacturing/operations or Research & Development/new product development is required.

KNOWLEDGE, SKILLS, ABILITIES and CERTIFICATIONS/LICENSES and LANGUAGES

Knowledge of Good Manufacturing Practice (GMP) and International Organization for Standardization (ISO) regulations preferred.
Project management experience required. Change management experience is preferred. Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is required.
Learning Management System (LMS) experience is preferred.
Knowledge of Process Excellence/Six Sigma tools and methodologies preferred.
Training within Industry Methodology (TWI), American Society for Quality (ASQ) and/or Process Excellence/Six Sigma certifications preferred.
Must have excellent communication, interpersonal and presentation skills.
Strong coaching and leadership skills.
Fluent in English and local language.

Certified in TWI (Training within Industry Methodology) is preferred
Experience working in a FDA and/or European regulatory environment is preferred.
Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001)
A thorough understanding of GMP (Good Manufacturing Practices)/ISO (International Organization for Standardization) regulations is preferred.
Project management abilities are required
Proficient in Microsoft Office —Word, Excel, and PowerPoint

BEOCS

Date Added: 10-01-2021

Chemical / Mechanical Engineer

15123

South San Francisco, California

Engineering

Overview:

Red line P & IDs CIP commissioning and troubleshooting SIP commissioning and troubleshooting
Piping walk downs
Turn over packages review Process troubleshooting
Data mining for troubleshooting or improvement purposes Help develop and maintain P & IDs throughout the project duration.
Review/comment on piping routing drawings, layout drawings, and Isometric drawings
Review/comment on instrument specification data sheets.
Support CIP/SIP design/commissioning/troubleshooting
Provide design support for Valve Array modifications.
Develop Equipment/Process Commissioning Documentation to support equipment changes.
Review/comment/support process IQ/OQ execution
Develop/Perform equipment/process studies to ensure equipment capabilities.
Work with vendors to ensure proper quality and timely delivery of equipment turnover packages.
Perform equipment calculations as necessary to procure equipment.
Work with support groups to provide training documentation on new equipment.
The engineer will focus on the configuration of the Basecamp 2.0 system.

The engineer will be responsible for data pertaining to areas of:

sites, process area, steps, activities, parameters, unit of measure, sampling, equipment, and template configurations.
They will need to compile feedback from pre-existing users and first-phase lessons learned to make updates that support business needs.

Skills

1-2 years experience in pharmaceutical or high tech experience, Clean utilities and or water purification, Project Manager or project engineer experience preferred.
Previous internship is ideal.

Education

Bachelor's of science in Engineering, preferrably Chemical or Mechanical.
Willing to accept resumes with Molecular Biology degrees/backgrounds as well.

BEOCS

Date Added: 10-01-2021

Global Studies Manager II

15122

South San Francisco, California

Biotech/R&D/Science

BEPC has South San Francisco, CA open position for Global Studies Manager to join our fast-growing team of consultants!

Contract W2 Period: 3 years with possibilities for extension
Pay & Benefits: pay/hr + Medical, Dental, Vision & Life Insurance
Location: 1 DNA Way South San Francisco California, United States

Ref: 15122 - ROCGJP00013199

WHAT YOU WILL DO:

As a Global Studies Manager (GSM), you will lead or contribute to one or more cross-functional global working groups, expert squads, and global Study Teams, which deliver all operational aspects of one or more studies through all phases and stages.

DRIVE OPERATIONAL EXCELLENCE

By developing operational plans, creating and managing clinical study budget and overseeing the consistency of operations.

MANAGE VENDORS AND STAKEHOLDERS

By managing relationships with vendors and cross-functional stakeholders. Oversee performance of vendors and third-party providers.

LEAD AND INFLUENCE

By establishing yourself as a leader within the team, being recognized as a thought leader who inspires others to perform at their best and learn from best practices.
You’ll be shaping our capabilities and evolving your role overtime.

MANAGE RISK AND COMPLIANCE

By developing site monitoring and risk mitigation strategies and ensuring your team adheres to all appropriate standards, including ICH/GCP and other regulations.

PLAN DEMAND AND SUPPLY

By overseeing the resource management, forecast and maintenance of supplies needed to ensure sites have the necessary supplies to run clinical studies.

PROVIDE COUNTRY OVERSIGHT

By leading feasibility assessments to ensure countries and sites are selected for participation in trials. Provide guidance to country operational reps during trials.

HOW YOU WILL DO IT:

You will succeed as a Global Studies Manager by leading, collaborating, and relaying your expertise to cross-functional partners. You will:
Apply your good knowledge of drug development process and respective regulations, including ICH and GCP guidelines
Apply your organizing and problem-solving skills to plan and run efficient operational aspects of a study
Motivate others to deliver against commitments, including leadership of global teams across diverse cultures and time zones, embracing diversity and creating a culture of inclusion to ensure successful collaboration
Demonstrate agility and ability to perform in a highly fast-paced, matrix environment where cross-team collaboration is crucial
Leverage excellent verbal and written communication skills to motivate your team, negotiate with peers and partners and influence across stakeholders
Advocate for what you and your team need to succeed
Model Roche’s values in everything you do

WHO YOU ARE

You are talented and passionate. You are inspired by our mission and would fit in well with our collaborative, rigorous and entrepreneurial spirit. You:

Have a growth mindset and are excited about learning through experience

Feel comfortable thinking on your feet and thrive in fast-paced, ambiguous and highly collaborative environments

Have a minimum 3 years of relevant experience (clinical trial management is a plus)

Hold a university degree or equivalent years of experience, preferred focus in life sciences

A self-starter who finds passion in achieving successful outcomes by leading, directing and inspiring peers

Want to make a difference and find excitement in innovating practices, products and processes

Possess strong working knowledge of drug development process and respective regulations, including ICH and GCP guidelines

BEOCS

Date Added: 10-01-2021

Senior Scientific Researcher

15120

South San Francisco, California

Biotech/R&D/Science

Sous Chef

15109

Lake Bluff, Illinois

Other Area(s)

Grill/Breakfast Cook

15108

Lake Bluff, Illinois

Other Area(s)

Drug Manufacturing Technician

15105

Des Plaines, Illinois

Other Area(s)

US - Manufacturing Engineer - G00554

15104

South Bend, Indiana

Engineering

BEPC Inc is looking for a Manufacturing Engineer in South Bend, IN!
Contract W2 Period: 6 months contract with possibilities for extensions
Pay & Benefits: $37.51/hr. +Medical, Dental, Vision and Life Insurance

Job Description

Work as part of a team by providing facilities management, manufacturing engineering, equipment readiness, equipment reliability, and operational activities at the South Bend site. You will be trained to become a process owner and subject matter expert within the Aerospace Wheel & Braking Systems Integrated Supply Chain team. As the Subject Matter Expert, you will be responsible to audit, train and certify operators on manufacturing operations of your assigned process. You will provide manufacturing expertise and ensure work instructions, manufacturing methods and equipment, equipment operability, workflow, and pre-established guidelines are followed to perform the operations of your assigned process.

Key Responsibilities

• Manufacturing Process Ownership
• Team coordination
• Coordinate resolution
• Process definition
• Project planning
• Mentor operators/technicians
• Drive technical solutions
• Communicate maintenance schedules
• Identify and prioritize work
• Approve and audit work
• Participate in planning
• Assist in outage planning
• Coordinate equipment readiness

YOU MUST HAVE

• Bachelors Degree in Engineering or Engineering Technology.

WE VALUE

• Ability to work independently
• Willingness to learn new technologies
• Mechanical Engineering experience
• Eagerness to get involved in hands-on work
• Proficient project management skills
• Good knowledge of the mechanical industry
• Cause identification/FMEA experience
• Working knowledge of SAP/HOS
• CAD system proficiency
• Ability to lead and direct the work of others.
• Extensive experience in facilities management or manufacturing.
• Strong analytical skills and creative thinking.
• Strong interpersonal and communication skills.
• Ability to work independently and in a team environment
• Fundamental mechanical aptitude and ability to troubleshoot equipment problems.

BEOCS

Date Added: 09-30-2021

Materials Handler I - 2nd Shift

15102

Temecula, California

Manufacturing

Technician

15101

Scarborough, Maine

Manufacturing

Service Operations Coordinator

15100

San Diego, California

Manufacturing

Production Planner I

15097

Westbrook, Maine

Manufacturing

Remote Supplier Quality Auditor

15095

San Angelo, Texas

Professional

BEPC has an open position for a Remote Supplier Quality Auditor!

Summary/Objective The Supplier Quality Auditor plans & conducts supplier quality system audits, both on site and remote desktop audits to applicable quality management system standards for fortune 500 Medical Device, Consumer and Pharmaceutical Companies.
The auditor conducts audits of suppliers across different industries such as Medical device, Pharmaceutical, Consumer, Biotechnology, Microbiology and Sterilization Sciences as needed to meet customer requirements.
The auditor must have the written and oral language skills to conduct supplier audits in English.

• Coordinates with suppliers to align on audit dates and conducts pre-audit planning including travel and accommodations where required.
• Performs audits to applicable QMS standards and regulations at the supplier’s site or remotely as required by the customer.
• Writes supplier audit reports to meet customer requirements.
• Updates audit tracking systems, e.g. EtQ for required audit updates.
• Reviews supplier audit corrective action plans for acceptance.
• Works with suppliers to have acceptable corrective action plans.
• Reviews objective evidence of supplier corrective actions for acceptance.
• Attends and participates in audit related meetings as required by customers. Other Duties Other duties may be assigned as required by BEPC management.

Competencies

• Must be able to effectively speak, write, and read in English.
• Thorough knowledge of QMS auditing principles and techniques
• Prior experience managing and performing quality management system audits to applicable standards and regulations such as ISO 9001, ISO 13485, 21CFR’s 820, 211, 4, 11
• Desirable: Ability to speak, write and read in additional languages such as Dutch, Portuguese, Italian and/or Chinese
• Leadership skills to work and collaborate with all levels of management
• Ability to be self-directed and work under minimal supervision
• Ability to build and maintain professional positive relationships with all groups
• Must have a “Can do” attitude
Must strive and be committed to “get the job done” and meet all deadlines
• Proficient in using Microsoft office tools such as MS Word and Excel • Ability to handle multiple and complex tasks.
Excellent written and verbal communication skills

Supervisory Responsibility

This position is an individual contributor position.

Work Environment

This job operates in a professional office environment.
This role routinely uses standard office equipment such as laptop computers and smartphones.

Position Type/Expected Hours of Work

This is a full-time position, and hours of work typically Monday through Friday, 8:00 a.m. to 5:00 p.m. However, agility and quick response time to customer and employee requests may be required at other times to include evening and weekends. This is a remote position and the candidate can be located in the US, Canada, Europe or other location. Travel Able to travel approximately 60% of time performing audits as required to meet customer & business needs.

Required Education and Experience

• Bachelor's degree in a technical field or engineering.
• 3 – 5 years’ experience auditing medical device companies and/or associated suppliers
• Quality system auditor qualifications preferred, e.g. ASQ CQA or CBA, ISO 9001/13485 lead auditor.

AAP/EEO Statement

BEPC Inc. policy is to affirmatively implement equal opportunity for all employees and applicants for employment without regard to race, color, religion, sex, national origin, disability, military status, genetic information, or any other basis prohibited by law. Additionally, BEPC Inc. does not discriminate against an employee or applicant who acts to oppose such discrimination or participates in the investigation of a complaint related to discriminatory employment practice. Employment decisions will be made on the basis of each applicant’s job qualifications, experience, and abilities.

Date Added: 09-29-2021

QA Specialist II

15094

Scarborough, Maine

Other Area(s)

BEPC Inc a great place to work, is searching for the correct candidate:

Q.A. Specialist II

This position is NonExempt. Hours over 40 will be paid at Time and a Half. Assures the quality of manufactured products and processes per standard operating processes(SOP'S) and GMP (Good Manufacturing Practices). BS degree or 3-7 years equivalent experience

Comments
Pay Rate of $75.00/hour for the right person.

The position of Quality Assurance Specialist II is within our Infectious Disease Developed Markets business unit located at Scarborough, Maine. In this role you will under minimal direction, the scope of this position is to perform a wide variety of activities to support the Quality Management System.

This job description will be reviewed periodically and is subject to change by management.

RESPONSIBILITIES:

Quality System Management

Review production batch records (DHR's) for accuracy and completeness in order to approve intermediate products for use in production. Review finished goods batch records. Report deviations in these records and assures these have been addressed and resolved prior to issuing approval.
Conduct spot-check inspections/audits of production operations
Participate in the internal audit program
Write, review and approve Standard Operating Procedures (SOPs) as necessary
Assist with and may write validations/test protocols as necessary
Assist in testing of complaint samples and stability samples and reports results out of acceptance limits
Provide backup to other Quality Specialists
Initiate and author Deviations and Quality Incidents (QI)
May administer the calibration program.
May administer the Document Control program
May administer the Deviation, Quality Incident and CAPA programs .
May organize the long term stability program and be responsible for administering the sample retention program.

May administer the Quality Records program and assist and act as backup to the Document Control Specialist II (with administrator rights in site electronic documentation system).
Train new and current Quality Assurance Technician and Specialists as needed
Other duties as assigned

Change Control Management

Change Management Documentation

o Assignment of Design History File numbers

o Compile and maintain quality system records associated with design change projects, including project definitions, first-lot-to-stock, product qualification records, etc.

o Ensure records for design change projects are complete and align with SOPs.

o Manage organization, storage, and archival of documentation and records associated with design changes and labeling.

Labeling Process Administration:

o Provide proofreading of product labeling prior to team review and approval.

o Initiate, execute and implement label changes in coordination with interdepartmental and external stakeholders.

Change Control Execution:

o Assist with implementation of product changes, in conjunction with project leads.

o Manage assigned Design Change projects (Typically associated with product labeling)

BASIC QUALIFICATIONS | EDUCATION:

Bachelor's Degree in Chemistry, Biology, Life Science, or other related technical field in a scientific or technical area or the equivalent combination of education and experience
Minimum three years in a Quality Assurance role for manufacturing.

PREFERRED QUALIFICATIONS:

3+ years prior experience in a Quality Assurance role or similar support role in the medical device industry.

COMPETENCIES:

Ability to follow procedures and accurately document results
Knowledge of site software for inventory management, Document Control and Quality incident tracking
Good working knowledge of Excel and Microsoft Word software
Ability to understand manufacturing processes of Company products and ability to recognize deviations from approved documented procedures

Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals
Ability to write routine reports and correspondence
Ability to speak effectively before groups of customers or employees of organization.
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
Ability to apply mathematical concepts such as fractions, percentages, ratios, and proportions to practical situations
Attention to detail

BEOCS

Date Added: 09-29-2021

Manufacturing Technician 1 (2nd Shift)

15093

Newark, Delaware

Manufacturing

Manufacturing Technician 1 (1st Shift)

15092

Newark, Delaware

Manufacturing

Materials Technician

15085

South San Francisco, California

Manufacturing

BEPC has an open position for a Materials Technician in South San Francisco, CA!

Contract W2 Period: 5 month contract with possibilities for extensions
Pay & Benefits: $21/hr. +Medical, Dental, Vision and Life Insurance

Under the supervision of the Materials operations supervisor, the Materials Specialist is responsible for the accurate receipt, verification, record keeping, distribution, and shipment of materials and goods. Work performed will include:

Acceptance of incoming materials by ensuring paperwork is accurate and materials are received in good conditions; prepare receiving documents
route receiving information
prepare outgoing shipments
observe proper handling storage and/or temperature requirements
provide for internal distribution of Good Manufacturing
Practices materials to company facilities
pack materials for proper shipping conditions
prepare shipping documents
prepare manifests for hazardous materials
perform x-ray scanning of packages
process and receive radioactive materials
apply proper placards
perform campus pick-up.s of outgoing shipments
apply asset tags to capital equipment
maintain equipment and work areas for cleanliness
operate material handling equipment in a safe and appropriate manner
Manage items that come to the warehouse and ensure proper sorting of inventory for support resue
Independently follows Current Good Manufacturing Practice procedures
clearly understands the importance of accurate GMP documentation;
observe all health and safety guidelines
Adjust to schedule changes, work overtime as necessary and float between groups as needed to support operations
Ensure that all work is completed by end of day. Utilize time wisely to maximize productivity
Serve as a liaison between customers and warehouse staff
Communicate clearly, both verbally and in writing
Meet timeline commitments and inform others of status, issues, and customer requests as necessary
Be punctual
Adheres to appropriate laws, GNE regulations and programs, and documentation procedures
Adhere to safety. Follow safety guidelines as required for your area
Complete training records in a timely manner.
Individual will be driving vans and/or bobtail trucks. Forklift certification is a plus. Individual will be driving on the streets.

Skills

Previous Experience with packaging equipment; Xray equipment
Attention to detail
Adherence to safety procedures
excellent communication skills
proficient in Word and Excel.
Warehouse and inventory experience
Strong organizational skills

BEOCS

Date Added: 09-29-2021

Labware Technician (MOLS)

15084

South San Francisco, California

Manufacturing

BEPC Inc is looking for a Labware Technician in South San Francisco, CA!
Contract W2 Period: 6 months contract with possibilities for extensions
Pay & Benefits: $19.00/hr. +Medical, Dental, Vision and Life Insurance

Job Description

Support the Lab Services department by working effectively within the group to meet department goals, objectives, and tasks to achieve desired results. Responsible for completing assigned tasks, which include cleaning, sterilizing, and prepping labware. Have knowledge of basic computer applications (Microsoft Word, Excel). Adhere to SOPs, cGMPs and other established procedures. Prioritize tasks and assignments to maximize efficiency and productivity.

Assigned Work and Support Tasks

Ensure distribution satellites are maintained with required inventory levels utilizing FIFO (First In-First Out).
Assist Lab Services Technicians as necessary.
Update labware deliveries on request system daily and complete assigned support tasks on time.
Provide routine updates to Supervisor/leads on progress, status, and issues associated with labware delivery and stock inventory status
Participate in process improvement initiatives and 5S as assigned.
Adjust to schedule changes, work overtime as necessary and float between groups as needed to support operations.
Ensure that all work is completed by end of day. Utilize time wisely to maximize productivity.
Serve as a liaison between customers and lab staff.
Communicate clearly, both verbally and in writing.
Meet timeline commitments and inform others of status, issues, and customer requests as necessary.
Be punctual.
Adheres to appropriate laws, GNE regulations and programs, and GMP documentation procedures.
Adhere to safety. Follow safety guidelines as required for your area.
Maintain own training through CHRIS LSO and attend at least 1 GMP training course per year. Complete training records in a timely manner.
May operate lab process equipment as necessary.
*Will drive a company vehicle
Valid CA driver's license required

Skills

Collaboration and Teamwork
People demonstrating this competency have a drive to work with peers, partners, and others, including individuals outside their own team and functional area to positively impact business performance and optimize the input of those involved.
Lab experience, particularly with use of Autoclaves.
Looks for opportunities to help others
Constructively accepts decisions made that are different than own view
Demonstrates respect and appreciation for diversity of perspectives and approaches among colleagues
Maintains professionalism in the presence of conflict
Offers productive and relevant views and information to impact decisions Driving for Results People demonstrating this competency drive for the achievement and improvement of business results, such results being broader in nature and with greater business impact at higher levels in the organization.
Responds to new requests with appropriate urgency and an organized approach
Holds self accountable to fulfill assigned tasks and achieve results within timelines
Asks for additional responsibilities or assignments when able * Analyzes and learns from mistakes

Education

College degree in Life Science is preferable
Candidate must have at least a high school degree

BEOCS

Date Added: 09-29-2021

Material Handler 1 (1st Shift)

15082

San Diego, California

Manufacturing

BEPC Inc is looking for a Materials Handler I in San Diego, CA!
Contract W2 Period: 5 months contract with possibilities for extensions
Pay & Benefits: $18.00/hr. +Medical, Dental, Vision and Life Insurance

** Mon- Fri 1^st Shift 7:30am – 4:30pm **

Duties and Responsibilities

Schedule packaging activities based on daily shipment priorities.
Package and label all outgoing products, product boxes and shipments.
Create and maintain packaging procedures.
Identify non-conforming materials or product.
Work with inventory control and shipping to insure prompt completion of packaging and shipping process.
Update routing steps in Oracle for material tracking.
Provide Support to shipping/receiving and stockroom
Correctly package all products according to packaging requirements.
Correctly label several product lines based on defined labeling requirements.
Prevent risks associated with shipping damage by properly following all defined procedures.
Prevent waste of materials.
Prevent material shortages or over stocking by close communication with inventory personnel.
Program temperature tracking devices.
Read and log results of incoming temperature logging devices.
Maintain individual work area/equipment in a neat, orderly manner.
This responsibility includes proper disposal of packaging waste, proper storage and use of equipment and parts, and management of documentation needed to perform duties identified within this job description.
Work with Manufacturing support groups to improve existing packaging operations methods and assist in the development of new methods.
Work well within a team environment.
Comply with all work safety rules and regulations.
Perform assembly of medical devices and decontamination of incoming medical devices requiring repair.

BEOCS

Date Added: 09-29-2021

Manufacturing Technician Specialist II

15081

Oceanside, California

Manufacturing

BEPC has an open position for a Manufacturing Technician Specialist in Oceanside, CA!

Contract W2 Period: 6 month contract with possibilities for extensions
Pay & Benefits: $47/hr. + Medical, Dental, Vision and Life Insurance

In this position, you will need to work effectively as part of a team responsible for ensuring successful and efficient pilot plant upstream/downstream operations and support of OCN site launching capability for the production of marketed recombinant proteins and their respective tech transfers.
The group conducts hands-on small scale and pilot plant operations with studies to continuously improve and optimize process performance, troubleshooting of our commercial scale make-assess-release, and supporting site tech transfers.
This individual must have the ability to adapt to rapidly changing priorities and has the flexibility to support small scale and pilot plant operations in accordance with the manufacturing and pilot plant schedule.

Responsibilities will include:

Perform routine small scale and pilot plant operations, including small scale and pilot scale media/buffers preparation, 20L bioreactor, 100L single-use bioreactor (SUB), 400L bioreactor, centrifuge, depth filtration system, and 500L SUB harvest hands-on operation, chromatography operations at small and pilot scale (AKTA), and UFDF operations at our pilot scale.
Support and perform cell perfusion operations
Clean-in-place (CIP) and steam-in-place (SIP) operations and perform any troubleshooting of the small and pilot plant equipment.
Support daily sampling, continuous trends and data monitoring, and assist in data analysis of small scale and pilot plant upstream and downstream data. Monitoring and analysis of manufacturing data as necessary.
Data design and execution of experiments aimed at improving process robustness/productivity or meeting the changing needs of the manufacturing environment.
Developing and implementing technologies that enhance our manufacturing operations. As with any position in a manufacturing environment, the job requires an ability to adapt to rapidly changing priorities and the flexibility to support operations in accordance with the manufacturing schedule.

Skills

Previous hands-on work experience in small scale laboratory and Pilot Plant upstream/downstream operations is highly desirable.
Proficiency in data analysis techniques, MS Office (i.e. Word, Excel, and PowerPoint), JMP statistical software tool, and basic laboratory skills, including aseptic technique is desirable.
Candidate should be highly motivated, be able to work independently, as well as in a team, and have good organizational skills.
Understands basic manufacturing, engineering and/or scientific theories, principles and techniques used in biopharmaceutical manufacturing processes and pilot plant operations.

Education

BS or higher degree required, in engineering and science related field (chemical engineering, biochemical engineering, molecular biology, biochemistry)

BEOCS

Date Added: 09-28-2021

CW Accounting Analyst

15080