Assistant Civil Designer

19814

Arizona, Arizona

Creative/Design

BEPC has an open position for an Assistant Civil Designer

Work location: Phoenix, AZ

Contract W2 Length 12-month contract with possibilities for extension.

Benefits: Medical, Vision, Dental, Life Insurance.

Shift: Monday - Friday 8:00AM- 5:00PM

Description:

Assistant Civil Designer will perform various phases of planning, proposal preparation technical layout and exhibit production support, site plan evaluations and exhibits, analytical designs, report exhibit preparation production, and preparation of construction drawings and environmental drawings as part of a project team. This position will work on various projects with a diverse portfolio of project types and clients. The following are the expectations for the position:

Responsibilities

Competent utilization and practical understanding of Autodesk’s Civil 3D and AutoCAD required.
Understanding and practical experience with MicroStation and Open Roads is a plus.
Support and perform technical design for civil engineering related projects requiring site plans, grading plans, access roads, driveways, storm drainage systems, storm water management facilities, water and sanitary sewer utility design, gas, electrical and communication utility design, sediment and erosion control, and roadway traffic control, and existing or new facility site design.
Develop drawings for production work including problem analysis, design layout and calculations on non-routine assignments of substantial variety and complexity.
Execute variety of civil design assignments for site plans, grading plans, and associated details using prescribed methods and standard techniques including drawing sequence and presentation, sizing various system components, and refining rough sketches.
Execute changes to designs or sketches and mark-ups on ongoing projects.
Analyze reports, maps, drawings, tests, and other topographical and geologic data to plan and design projects.
Responsible for incorporating appropriate design codes and specifications related to design requirements meeting generally accepted practices for civil engineering design.
Generate or review design drawings for quality assurance within communicated scope, budget, and schedule.
Calculate and report volume calculations for trench excavation and backfill, along with overall site grading.
Experience with developing balanced earthwork for projects is a plus.
Responsible for revisions of project drawings, plot files and project-related information storage in a logical and well-structured manner in accordance with communicated client standards.
Competent understand and utilization of Microsoft Office products to support calculations, development of design deliverables, and quantity calculations are required.
Other duties as assigned.

Requirements

Associate degree in drafting technology or related field and two years related experience or four years progressive detailing and design related experience.
Competent understanding and utilization of industry design software which includes Autodesk’s AutoCAD and Civil 3D, MicroStation and Open Roads, along with Microsoft Office products to develop, design and produce deliverables.
Novice knowledge in design, calculations, and design systems related to civil engineering discipline.
Novice knowledge in the theory and practices of civil engineering discipline
Novice knowledge in the fundamental concepts of other disciplines as they relate to the civil engineering discipline.
Capable of operating related discipline design software necessary to execute production tasks.
Ability to work collaboratively with others in a multi-discipline project team environment to resolve design or drawing issues as appropriate and to accomplish objectives.
Competent written & verbal communication skills.
Strong analytical and problem-solving skills, attention to detail and quality focused.

Travel. Yes, generally local utility plants, with potential to sites.

BEPRO

Date Added: 08-19-2022

Test Engineer

19813

Torrance, California

Engineering

BEPC has an open position for a Test Engineer in Torrance, CA!
Contract W2 Period: 6-month contract with possibilities for extensions
Pay & Benefits: Weekly Pay +Medical, Dental, Vision and Life Insurance

Requirements

Bachelor of Science in Engineering (Mechanical Engineering/Aerospace Engineering/Mechatronics Engineering)
Minimum of 4 years of experience in a Mechanical Test environment

Description:

Interacts with other engineering groups to define, document, analyze, perform, and interpret tests for products, systems, components, or modifications. Identifies functional problems and suggests resolutions. Assists in the definition of internal quality control standards and the maintenance of reliability programs. Analyzes test cases and provides regular progress reports. May require a bachelor's degree and 4-6 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 supervisor or manager.

Test Engineer (Mechanical) will be responsible for Reverse Engineering test equipment, documenting test system design, lab/facility interfaces, conducting development/production testing, commissioning, Test Plan and procedure development.

Key Responsibilities:

Reverse Engineer, Design, procure, fabricate, and maintain test equipment and facilities in support of Transition, development, demonstration, certification, and qualification tests.
Have experience with developing and interpretation of complex engineering drawings such as Test system schematics, wiring diagrams, wire harness drawings.
Experience Integration/testing of turbomachinery or equivalent test systems, Making changes and modifications to the Integrated test system.
Reverse Engineer Test equipment or testcarts and generate CAD Models & Production Quality Drawings
Manage scope, schedule, and budget for the assigned Test Program or Work Package, identifying requirements, risks and opportunities.
Monitor engineering progress against budget and forecasted schedule for the assigned test projects
Create Test Documentation (Test Procedures, Test Instructions, Instrumentation list, Piping and Instrumentation Diagram, Controls Architecture) in preparation for Test Solution commissioning and correlation process
Coordinate periodic reviews with management/Chief Engineer on project status, TRR,CDR,PDR and significant trends and changes of approved projects
Actively coordinates the design, implementation, commissioning, and maintenance of complex mechanical and control test facilities infrastructure required for aircraft components test and systems/subsystem integration test programs
Support estimates, Project planning and reporting for major test equipment and facility transition program.
Experience working with maintenance and upgrade of production and R&O test facilities.
Demonstrate strong project management skills (plan – execute – escalate).

We Value:

· Bachelor’s degree in Aerospace or Mechanical Engineering preferred
· Working knowledge of Turbomachinery, Aerodynamics.
· Aerospace component and systems test experience desired.
· Ability to develop, update Test system schematics, models and drawings
· Working knowledge of instrumentation and measurement systems desired.
· Demonstrated comfort working with complex systems (mechanical, fluid flow, hydraulics, pneumatics, data and automation).
· Demonstrated ability to work well with a team while being able to make decisions, balancing risks and rewards.
· Experience with Air Cooling Machines (ACM), Environmental Control System (ECS), the Poly Alpha Olefin (PAO) Pump systems, and the Electro Mechanical Power Systems (EMPS) is a plus.
· Experience in Project Management or basic training associated to Project Engineering tasks
· Basic knowledge of aircraft Bleed Air Systems, Environmental Control Systems, Auxiliary Power Systems, Power distribution Systems and/or Power Generation Systems

BEPRO

Date Added: 08-19-2022

Technical Recruiter

19812

Not Defined

Staffing

JOB DESCRIPTION

Summary/Objective
Recruiter will partner with the Managed Service Providers (MSP) and/or managers to anticipate and meet the evolving needs of the clients and to deliver best talent to their organization.This position primarily consists of selling contracts to candidates and obtaining qualified candidates to sell to clients. The position will nurture relationships with prospective talent and manage on-going manager relationships. The recruiter position is responsible for interviewing, testing and referring applicants for contract and direct hire positions within the industries we recruit for. This position must possess considerable skill in interviewing techniques, a good knowledge of all specialized functions in the company. An understanding of the company's organizational structure as well as an extensive knowledge of personnel policy and procedure and federal and state laws regarding employment practices.

Responsibilities

- Locate and interview candidates for our clients.
- Timely review of applicants who have applied via the applicant tracking system.
- Source candidates via resume databases and networking sites using Boolean search language.
- Solicit and pursue referrals from business networks and/or internal referrals.
- Articulate value proposition for candidates who are interested in the job opportunity.
- Prepare candidates for interviews; providing logistical information, interview schedule, and expectations for follow up from the recruiter.
- Ensure all candidates are provided with timely updates concerning the status of their applications and interviews.
- Conduct professional and thoughtful phone interviews.
- Compare candidate phone interview notes and skills assessments with requisition specifications to determine if the candidate is a match for the role.
- Continuously build talent pipeline to ensure there are multiple candidates in play at all times.
- Articulate a job offer and drives for candidate acceptance.
- Provide accurate and regular reporting of recruiting activities.
- Proactively and regularly communicated the status of each search to the hiring manager.

Other Duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Competencies

Customer/Client Focus.
Human Resources Capacity.
Problem Solving.
Thoroughness.
Time Management.
Building relationships

Supervisory Responsibility
This position has no supervisory responsibilities.

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 and days are Monday through Friday, 8:00 a.m. to 5:00 p.m. However, agility and quick response time to customer and employee request may be required at all times to include evening and weekends.

Classification

Non-Exempt

Travel
No travel is expected for this position.

Required Education and Experience

Associates Degree
Two years of experience in recruiting or sales

Preferred Education and Experience

Bachelor’s Degree in Marketing or Sales
One to two years of human resources experience; one to two years of human resources recruiting experience preferred

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.

BE OCS

Date Added: 08-19-2022

CW Learning Content Developer

19811

Plano, Texas

Creative/Design

BEPC has an open position for a Learning Content Developer

Location: Plano, TX Hybrid (mostly remote, once, or twice on-site in a month)
Requisition ID: 1137569
Contract Length: 6 month contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Reason for contingent headcount?

Current team is supporting a high-profile extensive initiative which requires additional development support to complete.

What is the project(s) name?

TPS for Admin Curriculum Development

What are the key objectives for this resource (project summary)?

Goal is to create learning elements like storyline files, Vyond videos, etc.

What You Will Be Doing:

Create holistic learning experiences in alignment with Academy foundational topics based on stakeholder requirements and acceptance criteria
Partner with Sr. Designers to execute on curriculum design strategy

Skills:

Advanced technical skill with development tools like Articulate, Adobe Creative Cloud, Vyond, Camtasia, SnagIt, Descript
Advanced technical skill with Audio/ Video production (record, edit, release)
Advanced skills and experience with the development of layered learning experiences covering multiple modalities, assessments

Experience:

5 - 10 years’ experience in Learning & Development, or Corporate Education
5 - 10 years creating learning content with a variety of development tools.
5 - 10 years creating curriculum and/or learning strategies in alignment with corporate business objectives.

Must Haves:

Advanced technical skill with development tools like Articulate, Adobe Creative Cloud, Vyond, Camtasia, SnagIt, Descript
Advanced technical skill with Audio/ Video production (record, edit, release)
Advanced skills and experience with the development of layered learning experiences covering multiple modalities, assessments

Preferred/ Nice-to-haves:

Advanced project management (Agile) skill (planning, prioritization, escalation, and delivery)
Graphic Design experience

BEPRO

Date Added: 08-19-2022

Environmental Cleaning Specialist

19808

Casa Grande, Arizona

Manufacturing

Senior Corporate Safety & Health Specialist

19807

Texas, Texas

Medical/Health

BEPC has an open position for a Senior Corporate Safety & Health Specialist in Fort Worth, TX

Contract W2 Period: 12 month contract with possibilities for extensions
Work location: Forth Worth, TX
Pay & Benefits: Medical, Dental, Vision and Life Insurance

Shift: Monday to Friday

Description:

- Plan and execute corporate and project Safety & Health initiatives in order to ensure a safe, healthy, and incident-free workplace.
- Lead the corporate and project safety policies and procedures while maintaining compliance processes applicable to the Local, State, and Federal Occupational Safety & Health Administration (OSHA) rules and regulations.
- Manage all aspects of Safety & Health at multiple project sites; to ensure contractual regulatory compliance by corporate employees and subcontractors.
- Lead Safety & Health personnel supporting field construction projects to assure operations are planned and conducted in a safe manner.
- Identify unique project specific Safety & Health issues for resolution. Provide advice, guidance, and direction to Site Safety personnel regarding safety and health issues and work practices.
- Create and validate project Safety & Health walk-through assessments. Monitor conformance to Safety & Health requirements to drive continuous improvement at the project site for any assessment findings.
- Document and resolve items that require immediate correction.
- Distribute specific Safety & Health information to corporate and project location.
- Generate memos relative to project safety and assist Site Safety personnel in the implementation of the site-specific safety and health program goals.
- Design & conduct on-site training required for project specific Safety & Health subjects to ensure compliance with the site specific Safety & Health Program and ensuring that the project training addresses all concerns with project personnel and subcontractors.
- Lead near misses, property damage, environmental incidents and accident investigation reporting, and the implementation of corrective measures as appropriate.
- Present to Corporate Safety & Health management periodically regarding the Project Safety & Health Program progress, challenges, and objectives.
- All other duties as assigned.

Requirements:

- Bachelor's degree in Occupational Health and Safety, Engineering, or Construction Management; and minimum 12 + years of experience in a construction field environment. Applicable experience may be substituted for the degree requirement.
- Knowledge of applicable electric utility transmission and distribution standards and work practices.
- Expert knowledge of Occupational Safety & Health Administration (OSHA), Construction and General Industry, America National Standards Institution (ANSI), National Institute for Occupational Safety & Health (NIOSH), Army Corps of Engineers (CoE), Engineers Manual 385-1 and National Electrical Code (NEC), Standards.
- OSHA 10 and/or 30 Hour Outreach Construction.
- Proficient in Windows-based platform and basic computer skills
- Previous experience actively working as Site Safety & Health representative on/at heavy industrial project locations preferred.
- This position requires driving to various locations; a valid driver's license is required.

BE PRO

Date Added: 08-18-2022

US - Safety Administrator

19806

Mason, Ohio

Professional

BEPC Inc is looking for a Safety Administrator in Mason, OH!
Contract W2 Period: 5 months contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

**Per Diem- $100 per day**

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.

Description:

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.

BEOCS

Date Added: 08-18-2022

Laboratory Technician

19805

Laramie, Wyoming

Manufacturing

Research Associate II

19804

South San Francisco, California

Biotech/R&D/Science

BEPC has an open position for a Research Associate II

Location: South San Francisco, CA
Requisition ID: ROCGJP00019036
Contract Length: 6 month contract with a possibility for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Research Associate II, Antibody Engineering

The Position:

The Antibody Engineering Department in Research and Early Development (gRED) is seeking a highly motivated and productive Research Associate. This individual will work on antibody discovery and characterization projects that support a variety of therapeutic pipeline programs and technology development. The individual will be involved in expanding our capabilities of antibody discovery and work on the design and engineering of novel modalities. The role will involve designing and conducting hands-on laboratory research and communicating those results to drive data-driven project decisions. Candidates with a passion for innovation and commitment to translational science are encouraged to apply.

Qualifications:

BS/MS in Biochemistry, Biophysics, Chemical Biology, or related disciplines with 2+ years of relevant lab experience.
Strong laboratory-based skills in molecular biology, protein biochemistry, and protein engineering.
Hands-on experience with in vitro display technologies (i.e. phage, yeast) is highly desired.
Prior research experience with antibodies or antibody-based molecules is a plus but not required.
Demonstrated ability to quickly learn new techniques, independently design experiments, and collect, analyze, interpret and present data.
Strong communication and interpersonal skills.
Detail-oriented and self-directed individual who is excited about tackling complex scientific challenges in a team-based setting.

BEOCS

Date Added: 08-18-2022

Warehouse Associate

19802

North Chicago, Illinois

Professional

Production Worker I

19801

Sturgis, Michigan

Manufacturing

Production Worker I

19800

Sturgis, Michigan

Manufacturing

Scientific Researcher

19799

South San Francisco, California

Biotech/R&D/Science

BEPC has an open position for a Scientific Researcher in South San Francisco, CA!!

Contract W2 Period: 2-year contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

The Position:
The Scientific Researcher performs laboratory-based activities and processes related to the tracking, inventory, preparation (DNA/RNA extractions) and transport of biological samples from clinical and non-clinical trials. This includes handling of associated metadata, coordination and execution of manual/and or automated sample processing workflows, request evaluation and ensuring that lab activities fulfill customer needs while achieving operational excellence in quality, service levels, cost and compliance.

Who are we looking for?
-Teamwork is a central part of how you love to function and thrive.
-You are looking to be part of a dynamic and growing organization where you want to influence your own development.
-You are curious and passionate about being an essential piece of the drug development process.

You bring:
• Scientific expertise combined with computational skills in relation to research
• Ability to independently design, execute and analyze complex sets of experiments or procedures and to recommend solutions when facing challenges
• Demonstrated experience in utilizing a variety of analytical platforms and instrumentation (such as liquid handling and automation, automated nucleic acid purification solutions). Prior experience with cell culture/ organoid culture and flow cytometry is a plus.
• Proven experience in leading projects, teams, and initiatives, delegation of activities and resolving issues as an escalation point
• Team player with strong interpersonal skills and the ability to build effective working relationships inside and outside their functional areas
• Experience assessing, tracking and fulfilling research customer needs on an operational level in an efficient and timely way with a high degree of customer orientation and ability to communicate with stakeholders on multiple levels. Prior experience in biobank-based processing laboratory experience is a plus.

Qualifications:
• Bachelors degree in Biotechnology, Cell Biology, Molecular Biology with 5 years industry or academy lab experience. Masters (MS) degree, in Biotechnology, Cell Biology, Molecular Biology with 3 years industry or academy lab experience.

• Following are some expectations for hands on laboratory experience (minimum 2-3 years):

1) DNA/ RNA extraction from human samples (blood tissue, stool).
2) Serum, plasma isolation from fresh human blood and aliquoting of the samples.
3) Handling human stool samples for various downstream processing.
4) Using LIMS system.

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. Full vaccination against COVID-19, defined as two weeks after final dose, is required for all contractors working onsite at Genentech facilities or leased facilities, unless otherwise exempt due to medical or religious accommodation. This is an ONSITE position.

BEOCS

Date Added: 08-17-2022

Scientific Researcher

19798

South San Francisco, California

Biotech/R&D/Science

BEPC has an open position for a Scientific Researcher!

Location: South San Francisco, CA
Requisition ID: ROCGJP00019038
Contract Length: 2 year contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

IMPORTANT: Client has mandated COVID-19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services are required to comply with this requirement. Full vaccination against COVID-19, defined as two weeks after final dose, is required for all contractors working onsite at the facilities or leased facilities, unless otherwise exempt due to medical or religious accommodation. This is an ONSITE position.

Description:

Scientific Researcher, Pharma Biosample Services

Seeking a creative and curiosity-driven Scientific Researcher to help in establishing tissue/ cell based sample processing services. The successful candidate will help in processing human blood, isolate PBMCs and support the Organoid team for tissue processing. This is a hands-on position involving close collaboration with an interdisciplinary team including colleagues from Safety Assessment team, Biomarker Development team, Research Pathology, and Bioinformatics.

Responsibilities:

Develop and apply multimodal single-cell processing techniques from various human tissue samples.
Optimize and execute complex tissue/sample processing
Effectively collaborate with cross-functional teams both within the department and across the company
Communicate results through scientific publications and presentations.
Contribute to lab organization and culture while helping to identify new research opportunities.

Qualifications:

Bachelor or Master degree in cancer biology, immunology, cell biology, genomics, bioengineering or a related discipline.
Minimum of 5 years total academic and/or industry hands-on lab experience required.
Hands-on expertise in tissue processing for single-cell/single-nucleus genomics applications is preferred.
Experience in technology development and optimization (wet lab and/or computational tools) is a plus.
Experience with primary cell culture and in vitro models is a plus.
Ability to manage multiple projects in parallel and collaborate with multidisciplinary teams.
Excellent communication, organizational, and collaboration skills along with demonstrated problem-solving abilities.

Who are we looking for?

Teamwork is a central part of how you love to function and thrive.
You are looking to be part of a dynamic and growing organization where you want to influence your own development.
You are curious and passionate about being an essential piece of the drug development process.
You bring Scientific expertise combined with computational skills in relation to research
Ability to independently design, execute and analyze complex sets of experiments or procedures and to recommend solutions when facing challenges
Demonstrated experience in utilizing a variety of analytical platforms and instrumentation (such as liquid handling and automation, automated nucleic acid purification solutions).
Prior experience with cell culture/ organoid culture and flow cytometry is a plus.
Proven experience in leading projects, teams, and initiatives, delegation of activities and resolving issues as an escalation point
Team player with strong interpersonal skills and the ability to build effective working relationships inside and outside their functional areas
Experience assessing, tracking and fulfilling research customer needs on an operational level in an efficient and timely way with a high degree of customer orientation and ability to communicate with stakeholders on multiple levels.
Prior experience in biobank-based processing laboratory experience is a plus.

BEOCS

Date Added: 08-17-2022

Senior Accountant

19797

Missouri, Missouri

Accounting/Finance

Research Associate III

19796

South San Francisco, California

Biotech/R&D/Science

BEPC has an open position for a Research Associate III in South San Francisco, CA!!

Contract W2 Period: 6-month contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

We are seeking an outstanding candidate to join the Biomolecular Resources Department. In this role, you will have the opportunity to be part of our state-of-the-art high throughput subcloning pipeline to generate DNA constructs for recombinant protein expression and cell engineering in support of basic research, Small and Large Molecule Drug Discovery.
The successful candidate will be responsible for generating DNA constructs in a timely manner through a combination of outsourcing and wetlab work, contributing to the advancements of the high throughput subcloning platform in a core facility setting using automated liquid handling systems and bioinformatics tools.
The ideal candidate will have deep expertise in standard and sophisticated Molecular Biology techniques and be able to partner with a variety of stakeholders throughout the organization.
They will also thrive on standardizing and simplifying methods to construct complex DNA constructs.
The successful candidate will be a team player with passion for quality work and timely delivery and enjoy working in a fast-pace, innovative environment.

Requirements:

Bachelors, or higher, degree in Biology/Biochemistry or a related scientific discipline with a minimum of 3 years experience, ideally in an industry or core facility setting.

Extensive hands-on experience with Molecular Biology techniques in high-throughput formats.

Detail oriented and comfortable in dealing with large data sets and distilling data to important points.

Familiarity with molecular biology software, such as Benchling, Geneious Prime.

Excellent agility to adapt to the changing needs and priorities for an organization to fulfill the business needs.

A team-oriented individual who recognizes the strengths of everyone on the team and appreciates diverse viewpoints.

Excellent communication, organization, time management and record keeping skills with a strong emphasis on data entry into the database.

Experience with liquid handling equipment is a plus.

Experience with protein expression is strongly desired.

BEOCS

Date Added: 08-17-2022

Plant Controller

19794

Not Defined

Professional

Ethicon, Inc in San Angelo, TX is looking for a Plant Controller to join their team!

Ethicon, Inc. based in Raritan, New Jersey, was founded more than 80 years ago as a pioneer in suture development and manufacturing, helping to transform the safety and effectiveness of open surgery. Ethicon Endo-Surgery, Inc. was created 20 years ago in Cincinnati, Ohio, developing innovative devices that have driven the revolutionary shift from open to minimally invasive surgery that continues to lead the industry today. Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer. The North America (NA) Ethicon Supply Chain Finance organization provides exceptional business leadership to bring value throughout the global supply chain as part of Johnson & Johnson’s MedTech sector. This position will be responsible for managing, coordinating, and controlling all finance & accounting related activities for the Manufacturing site in San Angelo, TX. This position will be a member of the San Angelo Leadership Team. Responsible for providing financial support, leadership, guidance in the long-term strategy for this site.

The Surgical Care business offers a broad range of products, platforms and technologies—including sutures, surgical staplers, clip appliers, trocars and synthetic mesh devices—that are used in a wide variety of minimally invasive and open surgical procedures.
Specialties include support for treatment of colorectal and thoracic conditions, women’s health conditions, hernias, cancer and obesity.
The Ethicon Surgical Care business combines products and services of two market-leading legacy companies, both with long histories of medical innovation.

Key Responsibilites:

• Directs, coordinates and controls all financial related activities at the manufacturing site.

• Oversee and monitor investment evaluations and expenditures.

• Implement control methods for fixed assets and inventory.

• Ensure plant management achieves financial commitments.

• Counsel and support department leadership to arrive at appropriate Credo based decisions.

• Direct the development of standard product cost based on specifications developed with production and planning personnel.

• Provides leadership and development for 3-person staff.

Qualifications - External

• A minimum of a bachelor’s degree is required, preferably in Finance, Accounting or business-related field.

• A MBA, CPA, CMA, or other financial certification is preferred.

• A minimum of 5 years’ experience in Accounting, Finance, or business-related field is required.

Statement of Work (PO) rev. 8/17/2022

Contingency Fee Page 10 of 12

• A minimum of 3 years’ experience in financial operations is preferred.

• Prior People management is required.

• Excellent communication and interpersonal relation skills is required.

• Supply Chain or Cost Accounting experience is required.

• Experience with JDE One World is preferred.

• This position will require up to 5% domestic and/or international travel.

• This position is in San Angelo, TX.

At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s

healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional, and financial

health of our employees and the ones they love. As such, candidates offered employment must show proof of COVID-19

vaccination or secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey

BEOCS

Date Added: 08-17-2022

Research Associate I

19793

South San Francisco, California

Biotech/R&D/Science

BEPC has an open position for a Research Associate I in South San Francisco, CA!!

Contract W2 Period: 1 year contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

This is for a contractor position as part of the Pathology Group in Safety Assessment. The candidate will be a highly motivated, independent person that will be primarily responsible in supporting necropsy activities with Safety Assessment. This will include, but are not limited to:
• Recording scientific observations during gross examinations
• Excising, weighing, and fixating tissues during necropsy
• Maintenance of study records
• Quality control of work and entering data in the department database
• Coordinating study logistics
The candidate will also be executing and coordinating the logistics of pathology samples for non-clinical studies conducted at Genentech. Those responsibilities will include, but are not limited to:
• lab setup
• Laboratory Information Management System (LIMS) data entry
• Pre-clinical sample handling and shipping preparation
• Handling of preserved tissue and preparation for histology processing

Must be able to sit or stand for extended periods. Must be comfortable performing some repetitive tasks such as block inventorying. Must be comfortable working in a highly interactive team setting and as such must exhibit excellent collaborative and communication skills within their team and with stakeholders. Microsoft Office and Google Apps knowledge required.

Skills
• Able to work in a fast-paced, highly interactive team environment.
• Animal handling and necropsy experience; proficient in comprehensive necropsy on rodents.
• Visual acuity to see small details during specimen examinations.
• Capable of operating independently to execute tasks at hand.
• Adherence to established policies, procedures and safety requirements.
• Ability to establish and maintain effective working relationships with fellow employees, management and clients.

Education

BS degree in animal sciences or similar field with a minimum of 1-2 years recent experience performing the procedures described above is required. AALAS certification is desired. Proven technical skills, strong interpersonal, communication (oral and written) and organizational skills are required. Must be able to lift at least 15 lbs. Work hours are commensurate with business needs.

BEOCS

Date Added: 08-17-2022

Technical Supervisor

19791

Santa Clara, California

Professional

BEPC Inc. is searching a Technical Supervisor in Santa Clara, CA.

CONTRACT W2: 12 – month contract with possibilities for extensions.

Job description:

The Supervisor will lead all aspects of technicians working on systems that maintain the supply of chemicals to a semiconductor manufacturing environment that makes the chips used in electronic devices such as Smart Phones, LEDs, and Flat Screen TVs. This is a meaningful, hands-on, exciting job opportunity for people who want to join a growing business.

This role is responsible for coordinating and supporting total gas and chemical management project, operations scheduling, execution, and completion activities and is a key customer interface for all operations, along with project-related and special requests.

• Drives safety-first culture with constant safety messages, communications, and team interaction to meet ZERO targets in safety and quality performance. Supervise BSP safety processes/requirements for shifts and assigned employees (spot checks).
• Drives a continuous improvement culture of making operational changes based on site needs and critical metrics. Responsible for implementing change across shifts; inspires change notification and compliance of changes across shifts.
• Works with other department interactions. Provides backup vacation relief in the absence of peers.
• Shift change responsibility reinforcement; ensures flawless handoff from shift-to-shift ensuring accurate communication on customer expectations and project deadlines.
• Main customer contact for all Operations and project activities. Drives accurate completion of all sustaining activities, maintaining ZERO gas or chemical interruptions.
• Communicates customer activity, such as reporting on delayed service requests, equipment reset status, and action item list completion.
• Trains and certifies technicians to attain the level of proficiency required to perform service in each of the skill areas according to the scope of work.
• Completes preventative and corrective maintenance and takes ownership of non-conforming events database (MAXIMO). Maintains online systems to address operational concerns in a timely manner reducing the amount of downtime.
• Performs 8D investigations with the use of the 8D problem-solving format. Conducts root cause investigations, develops and closes action items.
• Monitors and reports on any equipment or service excursion and performs appropriate escalation to customers.
• Maintains online shift schedule, supervises all attendance and performance-related issues, and delivers employee feedback as recommended or required.

Experience and education:

• 3+ years of experience in an Engineering, or Gas and Chemical manufacturing environment
• 3+ years of supervisory experience
• Bachelor’s Degree in Mechanical or Chemical Engineering or related field
• Previous semiconductor experience
• Solid understanding of gas and chemical systems and SEMI construction standards
• Previous project management experience in a fast-paced field
• Previous experience in MAXIMO or other maintenance database systems
• Proficient in Microsoft applications

Date Added: 08-17-2022

Gas and Chemical Technician

19790

Austin, Texas

Professional

BEPC Inc. is searching for a Gas and Chemical Technician in Austin, TX.

CONTRACT W2: 12 – month contract with possibilities for extensions.

** Different shifts available**

** OT available**

Job description:

If you have previous experience in Manufacturing, Gas and Oil, Chemical Technician, Industrial Mechanics, Production Technician, Bio-Tech, Automotive and Mechanics, Waste and Wastewater Treatment, Power Plant, or Refinery this could be a great fit for you!

Technicians work on systems and maintain the supply of chemicals and gases to a semiconductor manufacturing environment that makes the chips used in electronic devices such as Smart Phones, LEDs, and Flat Screen TV's
Technicians will be responsible for the safe operation of assigned chemical and/or gas distribution systems, with duties including:
• Handling and change-out of gas, chemical, and slurry containers
• Gas and chemical equipment troubleshooting and preventative/repair maintenance
• Computer operations to support job functions and customer needs
• Support of quality systems

Physical Attributes:
• Occasionally climbing ladders (utilizing fall protection)
• In some cases, Technicians must put on Supplied Contained Breathing Air Respirator (this type of respirator provides air from a cylinder through a mask connected to the cylinder) while working with chemicals (approx. 10-15 minutes).
• Basic lifting (up to 40lbs)
• Bending of the knees and overhead reaching
• PPE made available to workers include safety glasses, hard hat, ear plugs, chemical apron, gloves, etc. Worker will be provided with vouchers to purchase safety boots, which they are required to wear

Experience and education:
• High School Diploma or GED equivalent
• Prior experience in maintenance or as an equipment technician or in a mechanical or electronic environment is a plus
• Previous experience with chemical and gas distribution equipment is helpful but not a must
• Proficient with MS Office Suite
• Military training is welcomed
• Strong technical aptitude
• Excellent communication skills
Veterans from any branch or MOS with hands-on mechanical skill sets are encouraged to apply.

Date Added: 08-17-2022

Sr Advanced Mechanical Engineer

19787

Phoenix, Arizona

Engineering

Awareness Paid Media Manager, Canada

19786

Newark, New Jersey

Marketing

BEPC is seeking a talented Awareness Paid Media Manager for the Canadian Service team in Newark, NJ!

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

About the Role:
We are seeking a highly innovative marketer with a combination of proven strategic thinking and execution prowess to join the Canadian Service as a Marketing Manager on the Paid Media Acquisition team. You will have the unique opportunity to shape and define our Awareness Media strategies in order to successfully reach our brand awareness and consideration goals, as well as to support acquisition targets for this team. In particular, you will be responsible for working with our media agency to plan and execute our TV, online video (OLV), sponsorship, cinema, audio, and out of home (OOH) media buys. Additionally, a key strategic focus of this role is on OLV. You will work with our media agency and Google to deliver more memberships from our YouTube Video for Action campaigns, as well as acquisition focused OLV campaigns with native partners. As part of this role, you will work with our Manager, MAI to develop a holistic cross-channel video acquisition strategy across app campaigns, display, YouTube TrueView, and YouTube TrueView for Action.

The ideal candidate has had robust experience developing awareness-oriented paid media strategies for an entertainment company, particularly with OLV. The ideal candidate is innovative, collaborative, understands digital media, and translates industry and cultural trends into ideas to support our business. The role requires skills in both external and internal relationship management, cross-functional collaboration, and an ability to roll up your sleeves, as well as a passion for results, a commitment to action-oriented analysis, and a relentless focus on the customer. The right candidate will thrive in a highly entrepreneurial, fast-changing environment where people are driven, enthusiastic, collaborative and not afraid to take risks. This role is based in Newark, NJ, and reports to the Paid Media Marketing Director.

Key Job Responsibilities:

Partner with our media agency to develop our strategy for our TV, OLV, Sponsorship, Cinema, Audio, and OOH media buys.
Manage our awareness budget.
Brief the creative team on the assets we’ll need for our awareness media, ensuring to champion best practices by channel and to provide trackable click to action urls where applicable. Deliver post campaign insights and go forward recommendations for media optimizations.
Creative optimization on OLV, which includes identifying when we need new videos, working with the Creative team and our team intern to deliver new videos, and uploading the new videos to YouTube.
Partner with our media agency and Google to audit our OLV media campaigns, identifying best practices and areas of opportunity. Work with global colleagues to learn their best practices and improvement areas.
Deliver a strategic OLV awareness/consideration strategy based on a Google and media agency-driven audit, as well as global best practices.
Deliver a strategic OLV acquisition strategy, focusing on increasing new memberships from Video for Action campaigns and looking holistically across paid media video channels. This will also lean on best practices from Google and global colleagues.
Interpret and analyze data from multiple sources to inform channel decision making and propose new marketing ideas.
Run tests and optimizations to ensure incrementality with our media spend.
Stay up to date on digital media industry trends and industry activity in order to make recommendations.

Basic Qualifications:

B.A./B.S. required
5+ years of Awareness Paid Media experience, preferably in entertainment, subscription services, or at a media agency, managing a multi-million-dollar marketing budget across TV, OLV, Sponsorships, Cinema, Audio, and OOH.
Professional presence and communication skills with ability to multiple task across multiple priorities
Customer focused, creative, strategic, and analytical
Budget and forecasting management experience, including creating “what if” scenarios and distilling media trends and KPIs into a story
Ability to generate and quickly execute upon actionable recommendations based on the synthesis and analysis of data
Experience gathering and utilizing channel data and customer insights and turning these insights into successful marketing campaigns
Self-motivated, nimble and highly results-driven in a fast-paced and deadline-driven environment
A demonstrated record of partnering with teams across the organization and with external partners to achieve business results across multiple teams who may have different goals

Preferred Qualifications:

MBA or graduate degree.
Strong oral and written communication skills.
Strong understanding of subscription revenue business models.
Experience marketing in Canada, marketing in a dual-language marketplace, and fluency in French is a plus.

BEPRO

Date Added: 08-16-2022

Manufacturing Assembler / Operator 1 - Danvers/Taunton

19785

Danvers, Massachusetts

Manufacturing

BEPC has an open position for a Manufacturing Assembler / Operator 1

Work location: Danvers, MA

Contract W2 Length 12-month contract with possibilities for extension.

Benefits: Medical, Vision, Dental, Life Insurance.

Description:

Performs a variety of equipment operating and adjusting duties such as assembling, mixing, cleaning, welding, bonding, inspecting, testing, labeling, packaging, etc. to fabricate and process products to meet high quality specifications following prescribed procedures. Working from verbal and written instructions may use a variety of equipment including welders, hot air guns, scales, bonders, fillers, simple test equipment and other related supplies. May use measuring instruments to ensure conformance to specified tolerance disassembles precision assemblies and corrects malfunctions. Makes accept/reject decisions, taking corrective action where possible. Assignments are moderately complex, where judgment is required in solving problems and making recommendations. May involve choosing from two or more pre-defined alternative courses of action. Works under general supervision, with some instruction given for routine work and detailed instructions for new types of work or special projects

Qualifications:

Requires basic knowledge of how the team is organized and how own tasks relate to the others in the team/ unit. Impacts team performance through reliability and accuracy of own work.

High School diploma or GED equivalent

1-3 years of relevant work experience

Ability to read, follow and understand operating procedures

Ability to read, speak and understand instructions

Capable of doing basic math and counting to large numbers without error

Willingness to learn multiple production operations and adjust quickly to new tasks

Needs to be able to communicate effectively both in writing and verbally to report production information

Capable of working a full shift at a designated operation within the assigned manufacturing area}

Sufficient computer related skills to perform data entry and print reports

Works under close supervision at first and demonstrates the potential to work with less supervision over time

Essential Job Requirements:

Standing/reaching/bending/twisting/being able to lift 35 lbs.

BEOCS

Date Added: 08-16-2022

Manufacturing Assembler / Operator 1 - Danvers/Taunton

19784

Danvers, Massachusetts

Manufacturing

BEPC has an open position for a Manufacturing Assembler / Operator 1

Work location: Danvers, MA

Contract W2 Length 12-month contract with possibilities for extension.

Benefits: Medical, Vision, Dental, Life Insurance.

Description:

Qualifications:

Requires basic knowledge of how the team is organized and how own tasks relate to the others in the team/ unit. Impacts team performance through reliability and accuracy of own work.

High School diploma or GED equivalent

1-3 years of relevant work experience

Ability to read, follow and understand operating procedures

Ability to read, speak and understand instructions

Capable of doing basic math and counting to large numbers without error

Willingness to learn multiple production operations and adjust quickly to new tasks

Needs to be able to communicate effectively both in writing and verbally to report production information

Capable of working a full shift at a designated operation within the assigned manufacturing area}

Sufficient computer related skills to perform data entry and print reports

Works under close supervision at first and demonstrates the potential to work with less supervision over time

Essential Job Requirements:

Standing/reaching/bending/twisting/being able to lift 35 lbs.

BEOCS

BEPC has an open position for a Manufacturing Assembler / Operator 1

Work location: Danvers, MA

Contract W2 Length 12-month contract with possibilities for extension.

Benefits: Medical, Vision, Dental, Life Insurance.

Description:

Qualifications:

Requires basic knowledge of how the team is organized and how own tasks relate to the others in the team/ unit. Impacts team performance through reliability and accuracy of own work.

High School diploma or GED equivalent1-3 years of relevant work experience

Ability to read, follow and understand operating procedures

Ability to read, speak and understand instructions

Capable of doing basic math and counting to large numbers without error

Willingness to learn multiple production operations and adjust quickly to new tasks

Needs to be able to communicate effectively both in writing and verbally to report production information

Capable of working a full shift at a designated operation within the assigned manufacturing area}

Sufficient computer related skills to perform data entry and print reports

Works under close supervision at first and demonstrates the potential to work with less supervision over time

Essential Job Requirements:

Standing/reaching/bending/twisting/being able to lift 35 lbs.

BEOCS

Date Added: 08-16-2022

Engineering Project Manager- Robotics Program

19783

Hillsboro, Oregon

Project Management

Bepc, Inc has an opening for an Engineering Project Manager-Robotics Program in Hillsboro, OR!!
W2 Contract Period: 6-Months with possibilities of extensions
Benefits: Medical, Dental, Vision, Life Insurance

HTO Engineering Science &Technology (ES&T) is seeking a project manager to join their engineering team.
The Project Manager will be responsible for managing various projects within the business.
This person will work with members of ES&T engineering and other individuals in the value streams to deliver projects of various complexity and scope.
They will perform assigned tasks and work to achieve company goals and department objectives.
They will do all of the above while conforming to cGMP regulations and Genentech standards.
The Project Manager will report to the ES&T Engineering Manager.

Day shift work hours are flexible

Position is on-site

Responsibilities

Work with the site PMO, HLT and site leadership to prioritize projects on the site portfolio.
Identify, build and socialize resources for projects
Complete Capital Funding Requests for projects as required
Provide Project Updates to the Project Sponsor and Key Stakeholders
Complete Project Intake information for new projects
Manage and update the site portfolio for schedule, scope and budget updates using Service Now.
Identify and maintain project risk register as required.
Work cross functionally with commercial value stream members
Complete DARs as required to support project implementation
Work with commercial value streams to coordinate and schedule implementation activities
Build Work Breakdown Structures for projects and identify critical path activities.
Attend ES&T Engineering weekly SQDEC huddles as required.
Update work hours using SAP Fieldglass.
Complete GMP Training by required due dates
Create planned events as required within Veeva
Manage team meetings for projects
Capture meeting minutes as required
Provide engineering support such as document control
Insure the project team works safely at all times using pre-work safety briefings
Manage external contractors needed to support implementation tasks.

Qualifications

Bachelor of Science Degree in Engineering or related experience
Experience managing projects of various complexity in a manufacturing environment
Experience with robotics/automation technologies
Excellent communication skills
Strong collaborative skills
Ability to work in a self-directed capacity with minimal supervision
Strong leadership skills
Experience with MS Project or similar tool to manage projects
Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us.
Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.

Genentech requires all new hires to be fully vaccinated against COVID-19 as of their start date. This requirement is a condition of employment at Genentech, and it applies regardless of whether the position is located at a Genentech campus or is fully remote. If you are unable to receive the vaccine due to a disability or serious medical condition, or because it is prohibited as a result of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation.

BEOCS

Date Added: 08-16-2022

Operator I - 2nd Shift

19779

Temecula, California

Manufacturing

BEPC Inc is looking for an Operator I 2^nd Shift in Temecula, CA!
Contract W2 Period: 2 years contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Shift hours: 2:00pm – 10:30pm

Description:

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: 08-16-2022

Senior Piping Procurement Specialist

19777

Texas, Texas

Purchasing/Supply Chain

BEPC has an open position for a Procurement Piping Specialist!

Work location: Houston, TX

Contract W2 Length 12-month contract with possibilities for extension.

Benefits: Medical, Vision, Dental, Life Insurance.

Shift: Monday - Friday 8:00AM – 5:00PM

Description

The Senior Piping Procurement Specialist consults with management regarding the piping procurement and estimating aspects of projects. Leads the piping procurement activities by interfacing with the customer Global Practices, suppliers and clients.

Responsibilities

Responsible for leading the procurement of piping for projects.
Responsible for procurement of project required materials including manual valves, piping materials, piping specialty items, engineered pipe supports and pipe fabrication materials.
Manage contractual obligations and develop overall procurement strategies.
Provide innovative piping procurement solutions for clients and the company.
Manage official bid lists, bid documents, and bid tabs for all items estimated in Front End Planning (FEP) process.
Provide award recommendations to project management and procurement.
Develop and evaluate piping procurement efforts for major or critical projects.
Recommend proposed piping procurement services or technical applications when data is insufficient.
Mentor and train other staff members.
Source and prequalify new and/or prospective pipe fabricators and material suppliers to support project scope requirements.
Lead bid conditioning activities and facilitate pre-award negotiation meetings
Review and approve supplier invoices against contractual requirements.
Execute contract change orders as required by project.
Report on the development of project specific material expediting and supplier surveillance tasks.
Recommend new industry software and solutions for company and client use.
Develop and implement piping procurement strategies that align with company's diversity initiatives.

Requirements:

Bachelor's degree in Supply Chain Management, Law or Construction related field with a minimum of 14 years relevant experience required or relevant experience.
Experience working with or for a PVF supplier, mechanical contractor or EPC firm in the heavy process industry is required.
Must have advanced knowledge of current market conditions and suppliers.
Must be capable of applying extensive and diversified knowledge of principles and practices to broad areas of assignments and related fields.
Oracle Financial R12 software experience preferred.
Excellent written and verbal communication skills.
Excellent interpersonal skills.
Excellent negotiation skills.
Analytical and problem-solving skills.
Expert user of Microsoft Office.
Advanced user of Access Databases and Material Management Systems is required.

BEPRO

Date Added: 08-16-2022

Environmental Cleaning Specialist

19776

Columbus, Ohio

Food Services/Hospitality

Environmental Cleaning Specialist

19775

Columbus, Ohio

Manufacturing

Warehouse Associate - 2nd shift

19773

Irving, Texas

Manufacturing

Research Associate I

19771

Dixon, California

Biotech/R&D/Science

Engineer - Degreed III

19770

Alameda, California

Engineering

BEPC has an open position for Engineer Degree III in Alameda, CA!
Contract W2 Period: 12-Month contract with possibilities for extensions
Pay & Benefits: Weekly Pay +Medical, Dental, Vision and Life Insurance
100% on site

Requirements

Experience. in change management and business process mapping.

5+ years of experience.

Must have exp. in Business Process Mapping, Change Management, Facilitation, Coordination, Follow up

Certifications: Lean Six Sigma Black Belt or equivalent certification desirable. In absence of this

certification, experienced candidates who have worked in Operational Excellence or Business

Excellence roles with a proven track record will also be considered.

Responsibilities:

• Assisting leadership in timely and successful implementation of business excellence program.

• Create and sustain Operational Excellence (OpEx) initiatives such as Management Operating

System, Visual factory, Short Interval Control, Standard Work, etc.

• Continue to improve governance and control aspects of business processes

• Assist management to ensure all employees are participating in OpEx activities

• Identify opportunities for talent development and facilitate training programs for identified

skills.

• Define, collect, and report metrics. Facilitate identification of improvement opportunities with

relevant stakeholders.

• Map and document business processes and identify opportunities for improvement in

consultation with stakeholders.

• Design, develop, standardize, and implement Operational Excellence methods intended to

continuously improve system performance.

• Support all Company initiatives as identified by management

Ideal Candidate:

• This individual is an influencer and facilitator, with a track record of managing change.

• Collaborates with cross functional teams as required.

• Strong analytical, problem solving and project management skills

• Experience working in a broader enterprise/cross-division business unit model preferred.

• 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.

Date Added: 08-15-2022

Warehouse Associate

19769

Irving, Texas

Other Area(s)

Operator I

19766

Pleasanton, California

Manufacturing

BEPC has an open position for a Medical Device Assembler in Pleasanton CA!
Contract W2 Period: 4 month contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Full-time (shift: 6am-2:30pm)

DETAILS

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.

Education:
High school degree or equivalent preferred.

BEOCS

Date Added: 08-15-2022

Operator I

19765

Westbrook, Maine

Manufacturing

BEPC INC IS LOOKING FOR OPERATOR 1

WHERE: WESTBROOK ME

SHIFTS: 5:20 AM TO 4:55PM / 5:20 PM TO 4:55AM

BENEFITS: MEDICAL DENTAL VISION AND LIFE

CONTRACT: 4 MONTHS WITH EXTENSIONS OR PERMANENCY POSSIBILITIES

DESCRIPTION:

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

EDUCATION:

High school degree or equivalent preferred.

Date Added: 08-15-2022

Engineer - Degreed III_SJM

19764

Plano, Texas

Engineering

Sr. Quality Assurance Engineer

19763

Irving, Texas

Engineering

The role of the contract Sr. Quality Engineer is to participate with product/process teams to develop quality-engineered systems and products, support process validations, quality processes to ensure compliance with the company’s Quality System policies and procedures. Applicable external requirements and standards, including FDA, ISO 13485 and other worldwide regulatory agencies, Environmental, Health & Safety Practices, and other applicable standards as pertains to medical devices.

Drive quality assurance activities intended to ensure effective product quality processes are in place and carried out throughout lifecycle of product. May receive technical guidance on sophisticated problems, but independently settles and develops approaches and solutions.

RESPONSIBILITIES

Primary responsibilities include working in Quality Operations or Quality Engineering and with other functional groups in support of product/process.
- Using Quality tools/processes in development and implementation of practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecycle.
- Develop and establish effective quality control and associated risk management plans.
- Write, review and/or approve process and product validation protocols and reports, equipment qualifications, engineering change orders.
- Use statistical tools to analyze data, make acceptance decisions, and improve process capability (Six Sigma, SPC, DOE).
- Direct Failure Mode and Effects Analysis activities for Process FMEA’s.
- Provide all planning vital to ensure effective product acceptance. This includes, but is not limited to, part qualifications, specification development, and sampling plans.
- Support Supplier Quality as Quality Operations/Product Quality representative as appropriate.
- Conduct initiation, investigation, bounding, documentation, and review of non-conformances, CAPAs and customer complaints of quality issues as appropriate.
- Assist Regulatory Affairs in developing submissions for process changes, inspection changes, and new processes/devices as vital.
Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment when vital data are insufficient or confirmation by testing is advisable.
- Responsible for communicating business related issues or opportunities to next management level.
- Support Quality initiatives such as process and product characterizations that lead to continuous /cost improvements.
- Support or lead integration projects as needed.
- Perform other duties assigned as needed.

QUALIFICATIONS
A minimum of a Bachelor's degree in Engineering, Life Science, Physical Science or a related field is required; an advanced degree is an asset.

A minimum of 5 years Quality work experience is preferred, with experience in the medical device, pharmaceutical or other highly regulated industry also preferred.
Knowledge of ISO and/or cGMP regulations is preferred.
General knowledge in Quality Systems Regulations (QSR) is an asset.
An ASQ certification (CQE, CQM, CRE or CQA) is an asset.
Six Sigma (Green Belt, Black Belt, etc.) or Process Excellence certification is an asset.
Basic knowledge in Statistics, Sampling Planning, Risk Assessment and Process Validation is preferred.
Good communication and presentation skills will be needed.

Date Added: 08-15-2022

Ingredient Storage - Cleaning Specialist

19762

Altavista, Virginia

Manufacturing

Operator I

19761

Temecula, California

Manufacturing

BEPC Inc. is actively looking for a Operator in the Temecula, California area. 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.

EDUCATION: High school diploma or GED

LOCATION: On Site

DUTIES/RESPONSIBILITIES:

- 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.

BEOCS

Date Added: 08-15-2022

Safety and Quality Technician

19760

Austin, Texas

Technical

BEPC Inc. has a great job opportunity for a Safety and Quality Technician in Austin, TX!

W2 Contract for 12 months with opportunity for extensions.
Weekly pay and benefits: Medical, Dental, Vision and Life Insurance.

Job description:

This is a challenging, hands-on, and rewarding job opportunity for workers who want to join a growing business. Safety and Quality Technicians will be responsible for the safe operation of assigned chemical and/or gas distribution systems.

Technicians work on systems and maintain supply of chemicals and gases to a semiconductor manufacturing environment that makes the chips used in electronic devices such as Smart Phones, LED's, and Flat Screen TV's. They will ensure compliance in operation and maintenance procedures, and emergency preparedness, and drive flawless execution.

Core Responsibilities:

Developing and maintaining company inspection reports for safety and quality.
Auditing operations and maintenance areas according to quality and safety standards.
Ensuring processes and procedures comply with company standards as well as Federal and State law.
Validating all test equipment is calibrated and working correctly.
Reporting quality and safety issues immediately via the escalation process.
Collating test drafting quality and safety reports.
Assisting in root cause analysis investigation and resolution.
Identifying possible areas for improvement in quality control processes and safety.
Ensuring Operations is executing their task with Safety and Quality on each shift.

Some activities may require:

Walking approximately 5-6 miles per day.
Occasional climbing of ladders (utilizing fall protection).
Basic lifting (up to 40lbs).
Bending of the knees and overhead reaching.
PPE made available to workers includes safety glasses, hard hat, ear plugs, chemical apron, gloves, etc.
Worker will be provided with vouchers to purchase safety boots, which they are required to wear.
Technicians must put on Supplied Contained Breathing Air Respirator (this type of respirator provides air from a cylinder through a mask connected to the cylinder) while working with chemicals (approx. 10-15 minutes).

Shift Information:

Technicians will work compressed (12-hour shifts) of 3 days on, 3 days off / 4 days on, 4 days off, essentially meaning technicians have a lot of time off already built into their schedules. There is an opportunity for overtime.

Requirements:

High School Diploma or GED equivalent.
Safety / Quality Conscience – Root Cause and ISO Trained.
Technical degree or relevant technical training.
Problem-solving skills and Root Cause Analysis (5-Why, Fishbone, 4M, 5M or 6M).
Understanding of Health and Safety practices (Strong OSHA, DOT or PSM Experience).
Awareness of ISO9000 / ISO9001.
Analytical skills.
Proficient with MS Office Suite.
Failure Mode and Effect Analysis (FMEA).
Lean Manufacturing knowledge.
Knowledge of measurement.
Understanding of engineering drawings and manufacturing processes.
Planning and prioritizing activities.
Good communication and interpersonal skills.
Team working skills.
Ability to work on own initiative.

BEOCS

Date Added: 08-13-2022

Project Support - Production

19759

Casa Grande, Arizona

Manufacturing

Media Manager

19757

Newark, New Jersey

Marketing

BEPC is looking for a results-oriented Media Manager (contractor) in its Marketing team.

W2 Contract Period: 8+ months with possible extensions based on business needs and performance!

Listen up! There is a revolution afoot in entertainment and education!

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 our company 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: 08-12-2022

Warehouse Operations

19756

North Chicago, Illinois

Manufacturing

Logistics Specialist

19755

Vacaville, California

Biotech/R&D/Science

Bepc, Inc has an open position for a Logistics Specialist in Vacaville, CA!!
Contract W2 Period: 1 year with possibilities of extension
Benefits: Medical, Dental, Vision, Life Insurance

In this unique position, Pharmaceutical Materials Specialist are responsible for the execution of material logistics in a cGMP environment. This includes receiving, sampling, storage, issuance, distribution of materials/product and transfer. Handling and shipping of hazardous materials as required. Additional responsibilities include performing data entry into various databases, safely utilizing material handling equipment, adhering to cGMP procedures, ensuring department regulatory compliance, maintaining a clean and safe workplace.
.
Job Responsibilities
• Properly use all business and automation support systems (SAP, LIMS, EDMS, Trackwise, etc.)
• Safely operate materials handling equipment including forklifts and pallet jacks
• Identify issues through line-of-sight accountability. Inform Supervisor and receive guidance on issue resolution
• Identify and suggest ideas for improvements
• Proactively complete the required training and certifications (i.e., Forklift, Safety, Hazmat, cGMP)
• Strictly comply with cGMPs, SOPs, and Genentech Policies
• Escalate process issues as necessary to ensure resolution
• Communicate effectively and professionally in a team environment, be supportive of other team members
• Aware of corporate goals and direction in support of department and site initiatives. Support site strategies by actively contributing to department goal deliverables
• Aware of changes to requirements and able to adapt
• Adhere to all safety guidelines and procedures. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters safe work practices
• Receive and sample incoming raw materials and components into Vacaville's GMP warehouse.
• Prepare raw materials and components for shipment to other Genentech manufacturing sites
• Inventory and maintain minimum stock of raw materials/components in Vacaville manufacturing processing areas
• Prepare frozen bulk product for shipment to other Genentech manufacturing sites or CMOs
• Perform inventory, ordering, and storage of raw materials and supplies as required
• Maintain accurate documentation and raw materials inventory
• Perform scale/balance weight checks as required
• Process raw materials and components for return/rejection/destruction
• Complete inventory checks and cycle counts with goal of 100% inventory accuracy
• Handling, sampling, and internal distribution of hazardous materials
• Maintain equipment and work areas in a clean and orderly condition, always in an inspection ready state
• Perform miscellaneous materials handling duties when required

Job Requirements

Education:
• Associates Degree or equivalent combination of education and experience.

Experience
• Experience in computer-based systems and use in a validated environment preferred.
• Prior experience in a biotech, pharmaceutical, or chemical manufacturing environment preferred.

Knowledge/Skills/Competencies
• Prior training in chemicals handling, and good laboratory methods/practices preferred.
• Able to operate power industrial equipment (Forklifts) preferred.

Work Environment/Physical Demands/Safety Considerations

• Must be able to work weekends and overtime as required.
• Must be able to lift 40 lbs and stand for extended periods of time.
• Must have a valid driver license and clean DMV record.
• Ability to work in a highly cooperative team environment

BEOCS

Date Added: 08-12-2022

Senior Administrative Associate

19754

South San Francisco, California

Administrative

BEPC Inc. has a great job opportunity for a Senior Administrative Associate in South San Francisco, CA!

W2 Contract for 5 months with opportunity for extensions.
Weekly pay and benefits: Medical, Dental, Vision and Life Insurance.

Job description:

The Pharmaceutical Development (Pharm Dev) is responsible for developing pharmaceutical dosage forms, associated manufacturing processes and delivery technologies for investigational medicinal products (IMPs) and marketed products. Pharm Dev applies leading technical expertise to meet early-stage, late-stage, and commercial product needs.

The candidate will provide administrative support to the Leadership Team (Pharm Dev LT) composed of 6-9 members and carry some administrative responsibilities in support of the Pharm Dev functional excellence teams.

The successful candidate will:

Succeed not just by completing tasks, but also by proactively identifying and anticipating the needs of the LT members, effectively leveraging company resources, and demonstrating flexibility in planning work activities to maximize Pharm Dev productivity.
Have flexibility to handle a large volume of routine and non-routine work while providing a consistently accurate work product.
Have strong, positive interpersonal skills and experience working across cultures and with individuals at all levels of the organization.

Essential duties and responsibilities:

Manage multiple schedules including global (US, EU) meetings, and meeting with external parties.
Arrange, negotiate, coordinate and support meetings, events, and activities both on and off-site.
Organize, disseminate, and maintain documents and information, as per Pharm Dev best practices.
Develop, implement, and continuously improve administrative work processes, procedures, and systems; ensure compliance with Pharm Dev and company policies.
Collaborate closely with other admins in the organization, including backing up each other.
Work within the broader admin team within PTD South San Francisco to ensure aligned work practices and leverage them for peer-to-peer learning.
Manage deadlines related to business planning as well as other special projects

General office responsibilities include, but not limited to:

Schedule travel, and process payment and expense reports for sr. leaders in the organization, and facilitate obtaining travel documentation (e.g., visas)
Coordinate hiring process, including scheduling and managing interviews.
Coordinate onboarding/off-boarding and maintain org charts.
Manage visits by outside suppliers and contract manufacturers.
Create and prepare presentation materials.
Help setup contracts for consultants.
Processing purchase orders (POs), tracking invoices and associated interactions with Contracts and Finance groups.
Photocopying, distributing, and filing documents.
Document and data entry into on-line databases and document management systems.
Data entry into on-line resource management systems.
Maintain and update websites for various functional excellence teams and Pharm Dev.
Order Pharm Dev office supplies; maintain photocopying equipment; disseminate, mail, and organize (“5S”) / maintain mail/photocopy room.
Order catering and other supplies for a variety of meetings and events.
Track workspace allocation for Pharm Dev members.

Requirements:

BA or equivalent experience (at least 5 years previous senior level administrative experience).
Strong administrative organizational and technical skills that demonstrate attention to detail, ability to work independently and in teams, strong follow up skills, and ability to prioritize and manage multiple projects simultaneously.
Strong communication skills (email, professional writing and verbal) and ability to interact with people at various levels (entry level up to Sr. VP).
Experience in handling sensitive, confidential, and complex information.
Demonstrated problem solving and decision-making skills within agreed parameters.
Ability to type a minimum of 60 w.p.m.
Strong computer skills utilizing MS Word, PowerPoint, Excel, Google Apps (gMail, Docs, Sites, Drive, Calendar, Sheets, Forms, Slides, Hangouts), WebEx; experience with SharePoint or similar document management system
Interest and capability to learn various software systems used at the company for management of assets and resources.
Excellent written and verbal skills.

BEOCS

Date Added: 08-12-2022

Global Travel Program Manager

19753

Jersey City, New Jersey

Management

BEPC Inc is looking for a Global Travel Program Manager in Jersey City, NJ!
Contract W2 Period: 6 months contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Description:

Travel for Meetings This position is responsible for supporting and managing Global Travel for Meetings and Group Travel Programs for our global client.
The role will liaise and collaborate closely with Global Travel Manager and Global Meetings Manager including all relevant stakeholders and suppliers to ensure optimized delivery and program success.
The global program manager is the key point of contact for meeting planners, meeting program suppliers, and for traveler escalations, and is an embedded member into the Global Travel Program Management team.

Responsibilities include but are not limited to;
Operations

Intake/set up and manage new meetings/coordination with meeting planners and travel teams as appropriate, working to understand unique meeting requirements for the meeting / group travel request.
Set up of meeting technology tools such as OBT, GDS, registration tool support, and API reviews.
Support market-by-market mandatory MI set up as needed.
Responsible for airfare analysis and travel budget consults as needed
Lead role ensuring all regional / local GBT offices follow client travel policy, process and all MI POS requirements.
Key player in regional operational delivery, standard communications and local country TC training/staffing.
Key player in any standardization and operational improvement projects and implementation and management of meetings technology projects.
Provide Insights logistical reporting at the meeting level and support any regional reporting needs.
Contributing to client QBRs relating to the group air / travel for meetings program.

Regional relationship management

Support relationships with local client leadership and supporting 3rd party suppliers, client meeting owners.
Support relationship between client, suppliers, and GBT.
Align to Global Travel Program Management team as am embedded member.
Assess local market requirements and work solutions ensuring compliance with travel policy and gaining agreement and alignment between multiple stakeholders.

Communications

Effective & timely communication (written and verbal)
Communicate clear goals & objectives for initiatives and maintain open communications channels with timely status updates.
Effective use of Collaboration Spaces.
Understands escalation processes and is a confident decision maker.

Strategy Development

Provide valuable input which influences the shape and direction of the global travel for meetings strategy.
Create and maintain local level process flows.
Identifies and understands technology trends & tools in each market and the impact to travel program (online booking/meetings registration tools).
Conduct regional operational process reviews to optimize productivity.
Driving Results
Handles problems and acts on own initiative
Works proactively with operations to minimize impacts to front/mid/back-office tools due to technology changes
Improve standardization and adherence to travel policy through accurate reporting and use of MI.
Set clear objectives, defining key milestones to plan and organize workflow – create and manage a project plan.
Establish project plan and track progress against initiatives.
Work in collaboration with peers in implementing standardized servicing platform.

Requirements: Key Attributes

Sound knowledge of the meetings and travel industry
Strong communications skills (written and verbal)
Confidence to present and work with all members and levels of the organization
Proven ability to manage projects, multiple priorities, and effective time management
Effective use of Collaboration Spaces (i.e. SharePoint)
Working knowledge of Insights reporting tool
Prior group air/travel for meetings background
Strong knowledge of GDS, mid- and back office processes
High level understanding of meetings and travel technology trends and tools (i.e. online booking tools/meetings registration tools), globally and regionally
Ability to take external trends and assess impacts to the relevant stakeholder programs

BEOCS

Date Added: 08-12-2022

Inventory Control Analyst - G00552

19752

Clearwater, Florida

Logistics/Transportation

Operator I

19751

Westbrook, Maine

Manufacturing

BEPC has an open position for a Operator I

Work Location: Westbrook, Maine

Contract: W2 (contract length 4 Months)

Benefits: Medical health, Vision, Dental, Life Insurance (25k)

Shift: FLIGHT A Sunday thru Tuesday ALT Wednesday
Start time: 5:20a, 5:45a, 6:00a, 6:20a
End time: 4:55p, 5:20p, 5:35p, 5:55p

Description

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.

BEOCS

Date Added: 08-12-2022

Operator I

19750

Westbrook, Maine

Manufacturing

BEPC has an open position for an Operator in Westbrook, ME!
Contract W2 Period: 4-month contract with possibilities for extensions
Pay & Benefits: $25.00/hr. +Medical, Dental, Vision and Life Insurance

Description:

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.
Dress Code

Requirements:

Highschool Diploma or GED

BEOCS

Date Added: 08-12-2022

Medical Assembler Operator I

19749

Westbrook, Maine

Manufacturing

BEPC Inc. is urgently looking for a Medical Device Operator I in Westbrook, ME.

W2 CONTRACT: 4 – month contract with opportunities for extensions.

PAY AND BENEFITS: $25.00/ hr. + Medical, Dental, Vision and Life Insurance.

Flight A: 12 hr. shifts.

Job description:

This position is responsible for the production of high-quality medical COVID testing kits 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 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.

Experience:

High school degree or equivalent preferred.

BEOCS

Date Added: 08-12-2022

Operator I

19748

Westbrook, Maine

Manufacturing

BEPC has an open position for a Medical Device Assembler in Westbrook, ME!
Contract W2 Period: 4 month contract with possibilities for extensions
Pay & Benefits: Weekly Pay + Medical, Dental, Vision and Life Insurance

Full-time (3 days on, 4 days off/4 days on 3 days off)

DETAILS
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.

Education:
High school degree or equivalent preferred.

BEOCS

Date Added: 08-12-2022

Operator I

19747

Westbrook, Maine

Manufacturing

BEPC has an open position for a Operator in Westbrook, ME!
Contract W2 Period: 4 month contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Education: High School Diploma or GED equivalent.

DETAILS

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.

BEOCS

Date Added: 08-12-2022

Operator I

19746

Westbrook, Maine

Manufacturing

BEPC has an open position for an Operator I

Work location: Westbrook, ME
Contract W2 Length 3-month contract with possibilities for extension)

Shift: THURS-SAT, ALT WED -5PM-5AM/6PM-6PM/7PM-7AM

Description

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.

Responsibilities

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 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.

Basic Qualifications

High school degree or equivalent preferred.

Additional information

Required dress code for tour during interview and on-the job: Clothing must be non-shedding and free of frayed hems or loose threads. Tassels, fringes, glitter, sequins (sewn or glued on), and any other items that could become dislodges are not allowed on clothing. To verify a fabric can be worn: pull at the fabric tightly with fingers, if fibers are dislodged, the garment may not be worn in the production area. Sweaters, sweater vests, loose fiber garments, loose knit, or fleece may not be worn. All clothing must be clean and free of visible contamination (sand, mud, dirt, lint, etc.). All clothing, from the waist up, must fit under the lab coat/gown. Turtlenecks or high-necked clothing shall not stick out above the neck of the lab coat/gown. Sleeves shall not stick out beyond the cuff of the lab coat/gown. Caps, hats, scarves or bandanas shall not be worn under the bouffant. Head wraps/scarves worn to accommodate customs: Must be covered with the bouffant and the tail end of the scarf must be fully covered by the lab coat/gown. Must be of tightly woven fabric, be clean, and laundered. Loose fitting clothing shall not be worn around machinery or soldering/brazing torches. Shoes must be worn at all times in the production area. Stockings or socks are required. The heel of a shoe must not be pointed or higher than 2 inches. Sandals, clogs, slippers, open toe, or open heel shoes are not allowed. Shoes with straps or weave where toes can be seen are not allowed. Changing shoes in the production area, other than a gowning room, is not allowed. Torsos, upper arms, and legs must be covered. Pants (above the ankle), skirts (above the ankle), skirts with slits, short shirts (above the navel), and sleeveless tops are not allowed. Skirts at the ankle are allowed, but full-length stockings, leggings, or pants must be worn under them. Nail polish, acrylic, artificial nails, or similar nail coatings are not allowed. Jewelry or body piercings that can pierce gloves or cannot be covered under gowning materials will not be allowed in the production area. Makeup shall not be worn. Lip balm in stick form is acceptable, when applied outside of production areas and prior to hand washing. Scented personal use products shall not be worn, except deodorant. Lotions shall not be applied after hand washing. Cover any open or bleeding wound with a bandage. Don’t wear anything that could be offensive."

BEOCS

Date Added: 08-12-2022

Operator I

19745

Westbrook, Maine

Manufacturing

BEPC Inc. has a great job opportunity for an Operator I in Westbrook, ME!

W2 Contract for 3 months with opportunity for extensions.
Weekly pay and benefits: $24.20 – $28.20 per hour, plus Medical, Dental, Vision and Life Insurance.

Job description:

Essential duties:

Performs routine assignments according to specified and/or standardized procedures.
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 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.
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.

Flight D Shift:

Rotating working schedule, as indicated below:

Shift: 5:20 pm – 4:55 am, 5:45 pm – 5:20 am, 6:00 pm – 5:35 am, 6:20 pm – 5:55 am.

Week 1: Wednesday, Thursday, Friday, Saturday
Week 2: Thursday, Friday, Saturday.

Requirements:

High School Diploma or equivalent (GED)

Required dress code for tour during interview and on-the job.

BEOCS

Date Added: 08-12-2022

Manufacturing Assemble

19743

Danvers, Massachusetts

Other Area(s)

Operator 1

Danvers MA

W2 CONTRACT: 12 MONTHS WITH EXTENSION OR PERMANENCY POSSIBILITIES

WEEKLY PAY+ BENEFITS

DESCRIPTION:

Performs a variety of equipment operating and adjusting duties such as assembling, mixing, cleaning, welding, bonding, inspecting, testing, labeling, packaging, etc. to fabricate and process products to meet high quality specifications following prescribed procedures.
Working from verbal and written instructions may use a variety of equipment including welders, hot air guns, scales, bonders, fillers, simple test equipment and other related supplies.
May use measuring instruments to ensure conformance to specified tolerance disassembles precision assemblies and corrects malfunctions.
Makes accept/reject decisions, taking corrective action where possible.
Assignments are moderately complex, where judgment is required in solving problems and making recommendations.
May involve choosing from two or more pre-defined alternative courses of action.
Works under general supervision, with some instruction given for routine work and detailed instructions for new types of work or special projects.
Requires basic knowledge of how the team is organized and how own tasks relate to the others in the team/ unit.
Impacts team performance through reliability and accuracy of own work.

Requirements:

High School diploma or GED equivalent 1-3 years of relevant work experience
Ability to read, follow and understand operating procedures Ability to read, speak and understand English
Capable of doing basic math and counting to large numbers without error
Willingness to learn multiple production operations and adjust quickly to new tasks
Needs to be able to communicate effectively both in writing and verbally to report production information
Capable of working a full shift at a designated operation within the assigned manufacturing area Sufficient computer related skills to perform data entry and print reports
Works under close supervision at first and demonstrates the potential to work with less supervision over time

Job Requirements: Standing/reaching/bending/twisting/being able to lift 35 lbs.

Operator 1

Danvers MA

W2 CONTRACT: 12 MONTHS WITH EXTENSION OR PERMANENCY POSSIBILITIES

WEEKLY PAY+ BENEFITS

DESCRIPTION:

Performs a variety of equipment operating and adjusting duties such as assembling, mixing, cleaning, welding, bonding, inspecting, testing, labeling, packaging, etc. to fabricate and process products to meet high quality specifications following prescribed procedures.
Working from verbal and written instructions may use a variety of equipment including welders, hot air guns, scales, bonders, fillers, simple test equipment and other related supplies.
May use measuring instruments to ensure conformance to specified tolerance disassembles precision assemblies and corrects malfunctions.
Makes accept/reject decisions, taking corrective action where possible.
Assignments are moderately complex, where judgment is required in solving problems and making recommendations.
May involve choosing from two or more pre-defined alternative courses of action.
Works under general supervision, with some instruction given for routine work and detailed instructions for new types of work or special projects.
Requires basic knowledge of how the team is organized and how own tasks relate to the others in the team/ unit.
Impacts team performance through reliability and accuracy of own work.

Requirements:

High School diploma or GED equivalent 1-3 years of relevant work experience
Ability to read, follow and understand operating procedures Ability to read, speak and understand English
Capable of doing basic math and counting to large numbers without error
Willingness to learn multiple production operations and adjust quickly to new tasks
Needs to be able to communicate effectively both in writing and verbally to report production information
Capable of working a full shift at a designated operation within the assigned manufacturing area Sufficient computer related skills to perform data entry and print reports
Works under close supervision at first and demonstrates the potential to work with less supervision over time

Job Requirements: Standing/reaching/bending/twisting/being able to lift 35 lbs.

BEOCS

Date Added: 08-12-2022

US_Research Associate IV

19741

South San Francisco, California

Biotech/R&D/Science

BEPC has an open position for a Research Associate IV!

Location: South San Francisco, CA
Requisition ID: ROCGJP00018884
Contract Length: 6 month contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Duties:

The successful candidate will be involved in intracellular, extracellular or membrane bound protein purification from 1-10 Liter scale expressions from E coli, Insect cells, or Mammalian cells. They will also be expected to characterize protein quality using various biophysical and biochemical methods and participate in assay development to measure and compare reaction kinetics of relevant enzyme variants. In addition, the candidate will also be expected to perform mammalian cell culture work and optimize protocols to support exosome / extracellular vesicle isolation. This position will NOT be involved in antibody purification.

Skills:

Working knowledge of common protein expression systems such as mammalian, insect, E coli.
Expertise with modern protein purification and chromatography techniques, and knowledgeable with operating AKTA chromatography systems as well as analytical HPLC systems.
Direct experience with enzymology and assay development.
Basic mammalian cell culture (in particular suspension HEK293) experience.
Proficiency with methods to characterize protein quality and purity, such as mass spectrometry, SEC-MALS/DLS, endotoxin assays etc.
Expertise with biophysical and biochemical protein-protein interaction techniques and/or functional assays.
Experience with basic lab automation.
Passion for exploring and developing new technologies.
Self-motivated, hard-working, dynamic and curious person with good communication and problem-solving skills.
Team-oriented and collaborative nature.
Experience with structural biology techniques will be a plus, but not essential.
Experience isolating and characterizing extracellular vesicles / exosome is a plus but not essential.
Education:
The successful candidate must have either a BS/MS degree with ~6-10 years of experience or a PhD with 0-4 years of experience in Biochemistry, Chemical Biology, Structural Biology or a related discipline.

There is a potential for Full Time conversion with this position (not guaranteed).

BEOCS

Date Added: 08-12-2022

Sr Software Engineer

19740

Clearwater, Florida

Engineering

BEPC has an open position for Sr. Software Engineer in Clearwater, FL!
Contract W2 Period: 6-months contract with possibilities for extensions
Pay & Benefits: Weekly pay +Medical, Dental, Vision and Life Insurance
Remote role

MUST HAVE

• Bachelor’s degree in Engineering, Computer Science, Mathematics, or Physics
• 7+yrs of quantified experience in software engineering using ADA

Description:

REMOTE ROLE
Leading the full lifecycle develop of embedded real time safety critical navigational software. These solutions are defined from requirements, implemented in code, verified in simulation & hardware testing, and certified with government and safety organizations as part of Company’s Aerospace Products.

• Requirements decomposition and work assignments
• Sensor management & navigational feature definition & design
• Software architecture and coding of Realtime OS
• Integration & System activities
• Certification & Artifacts
• Unit Test & coordination of External Verification & Validation activities
• Factory deployment and support
• Ability to code in multiple languages

WE VALUE

• Understanding various software development lifecycle (waterfall, Agile)
• Demonstrate the ability to develop efficient and high-quality embedded software and architecture
§ DDC-I DeOS operating system
§ Inertial Sensor usage
§ GPS (SASSM or M-Code)
§ Kalman Filter implementation or optimization
• Developed software in certified or regulated safety environments (Ada)
§ DO-178 B/C process & artifact generation
§ OpenArbor Ada toolset
• Knowledge of software configuration management and change management practices
§ GIT / BitBucket
§ Jira
• Diverse and global teaming and collaboration
• Effective communicator
• Team leadership and coordination experience
• Can quickly analyze, incorporate, and apply new information and concepts
• Ability to consistently make timely decisions even in the face of complexity, balancing systematic analysis with decisiveness
• Ability to convey subtle or complex messages clearly, as appropriate for the topic and audience

BEPRO

Date Added: 08-11-2022

Material Handler

19738

Carmel, Indiana

Manufacturing

Process Engineering & Validation Expert 5

19737

Verona, Wisconsin

Engineering

Operator I

19736

Liberty, South Carolina

Manufacturing

BEPC has an open position for a Medical Device Assembler in Liberty, SC!
Contract W2 Period: 11 month contract with possibilities for extensions
Pay & Benefits: Weekly Pay + Medical, Dental, Vision and Life Insurance

Full-time (6 am-6pm Friday, Saturday, Sunday)

DETAILS
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.

Education:
High school degree or equivalent preferred.

BEOCS

Date Added: 08-11-2022

Materials Specialist

19734

South San Francisco, California

Manufacturing

BEPC has an open position for a Material Specialist!

Location: South San Francisco, CA
Requisition ID: ROCGJP00018912
Contract W2 Length: 6 month contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

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

**This role has the potential to convert to a full-time position
**This role is 100% On-Site.

Description of The Department:

gSupply is a partnered onsite supply stocking program for Research, supported by R&D Procurement & Lab Services. The onsite stocking program provides research associates with access to common products, saving time and effort. The consumable supply stocking service is supported throughout Research buildings.

Responsibilities:

The responsibilities for this position may include, but are not limited to:

Responsible for working with supervisors, leads, and other Material Specialists to ensure safe and quality operations while meeting operational goals.
Work effectively and efficiently in a team-oriented environment to keep Materials Operations running smooth and identify opportunities to improve procedures/operations.
Responsibilities include ensuring internal and external compliance (GMP, GLP, DOT, HazMat, etc.).
Adhering to health and safety guidelines.
Effectively executing Supervisor's directives.
Prioritizing and facilitating area tasks and daily customer requests.
Troubleshooting operational errors and monitoring operations.
Following up on facility/process/specialists needs.
Interacting with other departments to achieve goals, and acting as the liaison between the area Materials Specialists, Logistic Coordinators, Buyers, Inventory Analysts, and Supervisors.
Respond to customer inquiries via email, phone, and in person.
Prevent interruptions to customer processes by ensuring delays due to warehouse operations are minimized.
Attend departmental meetings as scheduled.
Serve as the main contact between customers and warehouse staff. Effectively represent areas to resolve issues with customers.
Be adaptive to changing priorities and responsibilities in all areas of Materials Operations.
Effectively multi-task the daily workload with assigned projects.
Routinely recognize and troubleshoot quality issues and follow-up with solutions
Through cross-training, become proficient in procedures and operations between other Materials Operations groups.
Seek out and participate in process improvement initiatives for warehouse functions, equipment, or procedures utilizing internal and external contacts and resources.
Ensure daily tasks are being completed accurately.
Ensure that incoming materials’ paperwork is correct and materials are received in good conditions.
Prepare to receive documents.
Prepare manifests for hazardous materials.
Route receiving information.
Perform x-ray scanning of packages.
Process and receive radioactive materials.
Apply asset tags to capital equipment.
Observe proper handling/storage/temperature requirements of materials.
Pack materials for proper shipping conditions, and prepare shipping documents.

Independently follow procedures and train others in all aspects of procedures.

Clearly understands the importance of accurate documentation.
Follow required safety procedures by using available safety equipment and participating in the safety awareness and training of staff.
Provide routine updates to Supervisors and leads on progress, status, and issues associated with the department.
Participate in projects and as needed deliver presentations to a diverse audience.
Actively participate in the development of departmental goals.
Engage in continuous feedback activities with supervisor including providing feedback when asked, soliciting constructive criticism, and initiating career development discussions.
Demonstrate the ability to work in a diverse environment with respect and professionalism.
Communicate clearly, both verbally and in writing.
Complete workload, assigned duties, and backup tasks on time.
Maintain equipment and work areas for cleanliness.
Understand and demonstrate proficiency with material handling equipment and relevant computer applications.
Ensure that all work is completed by end of the day. Utilize time wisely to maximize productivity.
Meet timeline commitments and inform others as necessary.
Adhere to appropriate laws, GNE regulations and programs, and DOT compliance.
Be punctual.
Ensure prior to performing duties, training is updated and compliant with regulations.
Meet all compliance requirements for training and complete training records and certifications in a timely manner.
Adhere to uniform dress code. Uniforms, if required, should be worn when interacting with customers.
Report damages to property or vehicles in a timely manner.
Assume leadership role in the absence of the Lead and/or Supervisor.
Provide training for staff and support retraining as procedures are created and updated. Assist in executing and monitoring a training plan for new personnel including ongoing feedback.

Requirements:

High School Diploma or GED.
Material handling and/or warehousing experience required.
Previous experience in leadership roles/responsibilities preferred.
Comfortable learning SAP and inventory management systems to receive and book materials.
Passion for continuous process improvement. LEAN or other Operational Excellence training and experience a plus.
Possess effective time management and organizational skills, ability to work independently, and demonstrate strong customer services skills.
Must possess good problem-solving and interpersonal skills.
Must communicate clearly and effectively.
Must have strong initiative and focus on safety, quality, accuracy, and be detail-oriented.
Knowledge of safe chemical handling is helpful.
Must possess a valid California driver’s license with a clean driving record; Class B and HazMat endorsement preferred.
Ability to drive forklifts
Potential lifting up to 40 lbs. and standing for extended periods of time.

BEOCS

Date Added: 08-11-2022

Clinical Supply Center Solution Prep Technician

19733

South San Francisco, California

Biotech/R&D/Science

Test Mfg Engineer

19732

Clearwater, Florida

Professional

Complaint Investigations Tech

19731

Alameda, California

Other Area(s)

US - Sr Adv Advanced Manufacturing Engineer

19729

Clearwater, Florida

Engineering

Operator I

19728

Westbrook, Maine

Manufacturing

BEPC Inc. is actively looking for a Operator for the 1^st shift in the Westbrook, Maine area. 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.

EDUCATION: High school diploma or GED

LOCATION: On Site

DUTIES/RESPONSIBILITIES:

- 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.

BEOCS

Date Added: 08-11-2022

Manufacturing Engineer

19726

Clearwater, Florida

Manufacturing

Manufacturing Engineer

19725

Clearwater, Florida

Engineering

US - Sr Electrical Technician

19720

Phoenix, Arizona

Technical

BEPC Inc is looking for a Sr Electrical Technician in Phoenix, AZ!
Contract W2 Period: 5 months contract with possibilities for extensions

High Preferences

Experience with IPC 610 highly desired
Experience Supporting defense programs
Experience Supporting avionics programs and Military Service
Aviation Experience

Description:

Responsible for assembling, troubleshooting, and producing aircraft avionics assemblies while adhering to pre-established guidelines and engineering specifications.
Requires a high school degree or its equivalent with at least 4-6 years of experience in the field or in a related area.
Familiar with standard concepts, practices, and procedures within a particular field.
Relies on experience and judgment to plan and accomplish goals.
Performs a variety of tasks.
Works under limited supervision.
A wide degree of creativity and latitude is required. Typically reports to a supervisor or manager. Experience in an electronics manufacturing shop floor environment and troubleshooting electronic products and test or manufacturing equipment a must.
Be part of a team that designs and develops test procedures and standards for highly complex products.
You will participate in the development and certification of test functionality across multiple products and applications
Have practical experience working with engineering equipment
Skills with trouble shooting and integrating products and test solutions using tools such as digital multimeters, oscilloscopes, logic analyzers.
Sound technical judgment and opinions.
Good interpersonal skills with ability to work effectively with other individuals in a team or project setting.
Individuals who are self-motivated and able to work with limited direct supervision.
Some experience in test support

BEOCS

Date Added: 08-11-2022

Complaint Investigations Tech

19717

Alameda, California

Technical

Material Handler

19716

Atlanta, Georgia

Manufacturing

Buyer (hybrid)

19715

Phoenix, Arizona

Purchasing/Supply Chain

Hybrid Schedule 3 days onsite/2 days remote a week.

MUST HAVE REQUIRED SKILLS:

- SAP experience
- Experience buying electronic components
- Aerospace experience
- Negotiations skills
- Self Starter

Job Description:

• Acting as a liaison between Sourcing and all other interfacing organizations to plan, coordinate and implement strategies for all Supply Chain activities related to fulfilling manufacturing and aftermarket requirements.
• Heavily involved in hardware transition activities including all aspects of planning and transition execution.
• Due to interface with global suppliers (time zone differences), the desirable candidate will need to be flexible on the hours worked.
• This individual plans, schedules, places orders and administrates purchase orders to ensure quality hardware is delivered on time.
• Maintains proper inventory levels per order policy. Interacts with personnel throughout the site with frequent outside contacts to discuss/negotiate difficult technical problems.
• Incumbent works under general direction with specified suppliers and hardware. Plans and schedules purchase orders in accordance with the production requirements as shown in the SAP ERP system.
• Manages inventory to a specified inventory plan as required to support the production schedule.
• Researches and provides constant feedback to department and management relative to material shortages and suppliers capacity and capabilities.
• Demonstrates an active commitment to continuous improvement in the areas of Quality, Cost, Delivery and Lead Time.
• Have effective interpersonal and communication skills with all levels of employees and management. High degree of confidence, objectivity, tact, diplomacy and ethical conduct is essential.
• Demonstrated ability in negotiations, planning and hardware administration procedures
• Ability to organize work, document and/or report concisely and accurately and be thorough in carrying out the responsibilities of the job.
• Monitor and release kits to both internal and external suppliers to support Production and After Market needs.
Responsible for purchasing and negotiating materials, equipment, and supplies from vendors.
Evaluates vendor quotes and services to determine most desirable suppliers.
May require a bachelor's degree or 1-3 years of experience in the field or in a related area.
Has knowledge of commonly-used concepts, practices, and procedures within a particular field.
Relies on instructions and pre-established guidelines to perform the functions of the job.
Works under immediate supervision.
Primary job functions do not typically require exercising independent judgment.
Typically reports to a supervisor or manager.

Date Added: 08-10-2022

Buyer

19713

Phoenix, Arizona

Professional

BEPC has an open position for a Buyer in Phoenix, AZ!
Contract W2 Period: 6 months contract with possibilities for extensions
Pay & Benefits: Weekly Pay +Medical, Dental, Vision and Life Insurance
Hybrid Schedule 3 days onsite/2 days remote a week.

MUST HAVE:

* Experience procuring Mechanical components (we are not electronic)
* Min. 3 Years of SAP experience
* Ability to interact and influence different business functions

PREFERRED REQUIREMENTS:

- Aerospace Experience
- Bachelor's degree or 1-3 years of experience in the field or in a related area
- Knowledge of commonly-used concepts, practices, and procedures within a particular field.

Job Description:

Acting as a liaison between Sourcing and all other interfacing organizations to plan, coordinate and implement strategies for all Supply Chain activities related to fulfilling manufacturing and aftermarket requirements.
Heavily involved in hardware transition activities including all aspects of planning and transition execution.
Due to interface with global suppliers (time zone differences), the desirable candidate will need to be flexible on the hours worked.
Plan, schedules, places orders and administrates purchase orders to ensure quality hardware is delivered on time.
Maintains proper inventory levels per order policy. Interacts with personnel throughout the site with frequent outside contacts to discuss/negotiate difficult technical problems.
Incumbent works under general direction with specified suppliers and hardware. Plans and schedules purchase orders in accordance with the production requirements as shown in the SAP ERP system.
Manages inventory to a specified inventory plan as required to support the production schedule.
Researches and provides constant feedback to department and management relative to material shortages and suppliers capacity and capabilities.
Demonstrates an active commitment to continuous improvement in the areas of Quality, Cost, Delivery and Lead Time.
Have effective interpersonal and communication skills with all levels of employees and management. High degree of confidence, objectivity, tact, diplomacy and ethical conduct is essential.
Demonstrated ability in negotiations, planning and hardware administration procedures
Ability to organize work, document and/or report concisely and accurately and be thorough in carrying out the responsibilities of the job.
Monitor and release kits to both internal and external suppliers to support Production and After Market needs.
Responsible for purchasing and negotiating materials, equipment, and supplies from vendors.
Evaluates vendor quotes and services to determine most desirable suppliers.
Relies on instructions and pre-established guidelines to perform the functions of the job.
Works under immediate supervision.
Primary job functions do not typically require exercising independent judgment.
Typically reports to a supervisor or manager.

Date Added: 08-10-2022

US - Buyer - G00540

19712

Phoenix, Arizona

Purchasing/Supply Chain

Hybrid Schedule 3 days onsite/2 days remote a week.

Job Description:
• Acting as a liaison between Sourcing and all other interfacing organizations to plan, coordinate and implement strategies for all Supply Chain activities related to fulfilling manufacturing and aftermarket requirements.
• Heavily involved in hardware transition activities including all aspects of planning and transition execution.
• Due to interface with global suppliers (time zone differences), the desirable candidate will need to be flexible on the hours worked.
• This individual plans, schedules, places orders and administrates purchase orders to ensure quality hardware is delivered on time.
• Maintains proper inventory levels per order policy. Interacts with personnel throughout the site with frequent outside contacts to discuss/negotiate difficult technical problems.
• Incumbent works under general direction with specified suppliers and hardware. Plans and schedules purchase orders in accordance with the production requirements as shown in the SAP ERP system.
• Manages inventory to a specified inventory plan as required to support the production schedule.
• Researches and provides constant feedback to department and management relative to material shortages and suppliers capacity and capabilities.
• Demonstrates an active commitment to continuous improvement in the areas of Quality, Cost, Delivery and Lead Time.
• Have effective interpersonal and communication skills with all levels of employees and management. High degree of confidence, objectivity, tact, diplomacy and ethical conduct is essential.
• Demonstrated ability in negotiations, planning and hardware administration procedures
• Ability to organize work, document and/or report concisely and accurately and be thorough in carrying out the responsibilities of the job.
• Monitor and release kits to both internal and external suppliers to support Production and After Market needs.

Responsible for purchasing and negotiating materials, equipment, and supplies from vendors.
Evaluates vendor quotes and services to determine most desirable suppliers.
May require a bachelor's degree or 1-3 years of experience in the field or in a related area.
Has knowledge of commonly-used concepts, practices, and procedures within a particular field.
Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision.
Primary job functions do not typically require exercising independent judgment.
Typically reports to a supervisor or manager.

Date Added: 08-10-2022

Buyer

19711

Phoenix, Arizona

Professional

BEPC has an open position for a Buyer in Phoenix, AZ!
Contract W2 Period: 6 months contract with possibilities for extensions
Pay & Benefits: Weekly Pay +Medical, Dental, Vision and Life Insurance
Hybrid Schedule 3 days onsite/2 days remote a week.

MUST HAVE SKILLS:

- Purchasing experience
- MRP knowledge
- MS Office (especially Excel)

PREFERRED SKILLS:

- SAP experience
- Aerospace experience
- Negotiations skills

Job Description:

• Acting as a liaison between Sourcing and all other interfacing organizations to plan, coordinate and implement strategies for all Supply Chain activities related to fulfilling manufacturing and aftermarket requirements.
• Heavily involved in hardware transition activities including all aspects of planning and transition execution.
• Due to interface with global suppliers (time zone differences), the desirable candidate will need to be flexible on the hours worked.
• This individual plans, schedules, places orders and administrates purchase orders to ensure quality hardware is delivered on time.
• Maintains proper inventory levels per order policy. Interacts with personnel throughout the site with frequent outside contacts to discuss/negotiate difficult technical problems.
• Incumbent works under general direction with specified suppliers and hardware. Plans and schedules purchase orders in accordance with the production requirements as shown in the SAP ERP system.
• Manages inventory to a specified inventory plan as required to support the production schedule.
• Researches and provides constant feedback to department and management relative to material shortages and supplier’s capacity and capabilities.
• Demonstrates an active commitment to continuous improvement in the areas of Quality, Cost, Delivery and Lead Time.
• Have effective interpersonal and communication skills with all levels of employees and management. High degree of confidence, objectivity, tact, diplomacy and ethical conduct is essential.
• Demonstrated ability in negotiations, planning and hardware administration procedures
• Ability to organize work, document and/or report concisely and accurately and be thorough in carrying out the responsibilities of the job.
• Monitor and release kits to both internal and external suppliers to support Production and After Market needs.

Responsible for purchasing and negotiating materials, equipment, and supplies from vendors. Evaluates vendor quotes and services to determine most desirable suppliers. May require a bachelor's degree or 1-3 years of experience in the field or in a related area. Has knowledge of commonly used concepts, practices, and procedures within a particular field. Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. Primary job functions do not typically require exercising independent judgment. Typically reports to a supervisor or manager.

Date Added: 08-10-2022

Buyer (hybrid)

19710

Phoenix, Arizona

Purchasing/Supply Chain

Hybrid Schedule 3 days onsite/2 days remote a week.

Job Description:
• Acting as a liaison between Sourcing and all other interfacing organizations to plan, coordinate and implement strategies for all Supply Chain activities related to fulfilling manufacturing and aftermarket requirements.
• Heavily involved in hardware transition activities including all aspects of planning and transition execution.
• Due to interface with global suppliers (time zone differences), the desirable candidate will need to be flexible on the hours worked.
• This individual plans, schedules, places orders and administrates purchase orders to ensure quality hardware is delivered on time.
• Maintains proper inventory levels per order policy. Interacts with personnel throughout the site with frequent outside contacts to discuss/negotiate difficult technical problems.
• Incumbent works under general direction with specified suppliers and hardware. Plans and schedules purchase orders in accordance with the production requirements as shown in the SAP ERP system.
• Manages inventory to a specified inventory plan as required to support the production schedule.
• Researches and provides constant feedback to department and management relative to material shortages and suppliers capacity and capabilities.
• Demonstrates an active commitment to continuous improvement in the areas of Quality, Cost, Delivery and Lead Time.
• Have effective interpersonal and communication skills with all levels of employees and management. High degree of confidence, objectivity, tact, diplomacy and ethical conduct is essential.
• Demonstrated ability in negotiations, planning and hardware administration procedures
• Ability to organize work, document and/or report concisely and accurately and be thorough in carrying out the responsibilities of the job.
• Monitor and release kits to both internal and external suppliers to support Production and After Market needs.

Responsible for purchasing and negotiating materials, equipment, and supplies from vendors. Evaluates vendor quotes and services to determine most desirable suppliers. May require a bachelor's degree or 1-3 years of experience in the field or in a related area. Has knowledge of commonly-used concepts, practices, and procedures within a particular field. Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. Primary job functions do not typically require exercising independent judgment. Typically reports to a supervisor or manager.

Date Added: 08-10-2022

Buyer (hybrid)

19709

Urbana, Ohio

Purchasing/Supply Chain

Hybrid Schedule 3 days onsite/2 days remote a week.

Job Description:
• Acting as a liaison between Sourcing and all other interfacing organizations to plan, coordinate and implement strategies for all Supply Chain activities related to fulfilling manufacturing and aftermarket requirements.
• Heavily involved in hardware transition activities including all aspects of planning and transition execution.
• Due to interface with global suppliers (time zone differences), the desirable candidate will need to be flexible on the hours worked.
• This individual plans, schedules, places orders and administrates purchase orders to ensure quality hardware is delivered on time.
• Maintains proper inventory levels per order policy. Interacts with personnel throughout the site with frequent outside contacts to discuss/negotiate difficult technical problems.
• Incumbent works under general direction with specified suppliers and hardware. Plans and schedules purchase orders in accordance with the production requirements as shown in the SAP ERP system.
• Manages inventory to a specified inventory plan as required to support the production schedule.
• Researches and provides constant feedback to department and management relative to material shortages and suppliers capacity and capabilities.
• Demonstrates an active commitment to continuous improvement in the areas of Quality, Cost, Delivery and Lead Time.
• Have effective interpersonal and communication skills with all levels of employees and management. High degree of confidence, objectivity, tact, diplomacy and ethical conduct is essential.
• Demonstrated ability in negotiations, planning and hardware administration procedures
• Ability to organize work, document and/or report concisely and accurately and be thorough in carrying out the responsibilities of the job.
• Monitor and release kits to both internal and external suppliers to support Production and After Market needs.

Responsible for purchasing and negotiating materials, equipment, and supplies from vendors. Evaluates vendor quotes and services to determine most desirable suppliers. May require a bachelor's degree or 1-3 years of experience in the field or in a related area. Has knowledge of commonly-used concepts, practices, and procedures within a particular field. Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. Primary job functions do not typically require exercising independent judgment. Typically reports to a supervisor or manager.

Date Added: 08-10-2022

Engineer - Degreed III

19708

Alameda, California

Engineering

CAD Designer

19706

Kansas City , Missouri

Professional

Staff Mechanical Engineer

19705

Kansas City, Missouri

Professional

BEPC Inc. is searching for a Staff Mechanical Engineer in Kansas City, MO.

CONTRACT W2: 2 – month contract with possibilities for extensions.

Job description:

The Staff Mechanical Engineer will lead computational fluid dynamics (CFD) design project to create world class designs for new projects, alterations, and redevelopments on a variety of projects including power, process, corporate, healthcare, pipeline, airports, institutional, industrial, manufacturing, government, and military facilities. Regular meetings with the CFD Team Manager will be required for resource and project completion planning.

Lead CFD analysis of projects from the conceptual phase through design completion for project needs and requirements that are set forth by the project managers.
Applies expert knowledge of commonly used CFD concepts, practices, and procedures within the CFD services industry.
Applies knowledge and experience to complex projects, find non-standard design solutions.
Quality review production CFD models for a variety of projects and project related data as required by the project managers to verify corrections are made within multiple CFD and CAD related software.
Prepare and present technical reports for clients and industry publications.
Build effective relationships with existing clients, customers and contractors and develop new business opportunities. Responsible for ensuring customer satisfaction goals and expectations are met.
Participate sales and marketing efforts and identify key pursuits.
Responsible for QA/QC process adherence.
Responsible for effective communication with other engineering disciplines.

Experience and education:

Bachelor's degree in engineering from an accredited program. Master's level is preferred.
Minimum 4 years related professional experience in CFD analysis.
Must demonstrate excellent oral and written communication skills, strong interpersonal skills, and the ability to clearly and effectively present complex information to all levels of employees, management, and clients.
Strong analytical and problem-solving skills. This position requires an individual capable of applying intensive and diversified knowledge of principles and practices to fluid and thermal analysis of building thermal management systems, external flow modeling of buildings and cooling towers, clean room spaces, and various other fluid systems.
Experience in steady-state and transient CFD modeling is required.
Experience with battery energy storage systems, data centers, and clean manufacturing spaces is a plus.
Capable of devising new approaches to problems encountered.
Experience with Autodesk CFD or Ansys Fluent products is preferred.
Experience with Revit, Autocad or similar 3D modeling software is preferred.

Must be expert in the use of computer software (i.e., Microsoft Word, Excel, PowerPoint).

BEPRO

Date Added: 08-10-2022

Principal Systems Engineer

19704

Minneapolis, Minnesota

IT/Software Development

REMOTE Lead Software Engineer

19703

Clearwater, Florida

IT/Software Development

Leading the full lifecycle develop of embedded real time safety critical navigational software. These solutions are defined from requirements, implemented in code, verified in simulation & hardware testing, and certified with government and safety organizations as part of Honeywells Aerospace Products.
• Requirements decomposition and work assignments
• Sensor management & navigational feature definition & design
• Software architecture and coding of Realtime OS
• Integration & System activities
• Certification & Artifacts
• Unit Test & coordination of External Verification & Validation activities
• Factory deployment and support
• Ability to code in multiple languages

YOU MUST HAVE
• Bachelors degree in Engineering, Computer Science, Mathematics, or Physics
• 7+yrs of quantified experience in software engineering using ADA

WE VALUE
• Understanding various software development lifecycle (waterfall, Agile)
• Demonstrate the ability to develop efficient and high-quality embedded software and architecture
DDC-I DeOS operating system
Endian swap and other porting activities (Ada)
Integration of software into test stations (Ada & C/C++)
Inertial Sensor & GPS usage
Kalman Filter implementation or optimization
• Developed software in certified or regulated safety environments (Ada)
OpenArbor Ada toolset
• Knowledge of software configuration management and change management practices
GIT / BitBucket
Jira
• Diverse and global teaming and collaboration
• Effective communicator
• Team leadership and coordination experience
• Can quickly analyze, incorporate, and apply new information and concepts
• Ability to consistently make timely decisions even in the face of complexity, balancing systematic analysis with decisiveness
• Ability to convey subtle or complex messages clearly, as appropriate for the topic and audience

Date Added: 08-10-2022

Operator I - 2nd Shift

19701

Liberty, South Carolina

Manufacturing

BEPC has an open position for an Operator I - 2nd Shift

Work location: Pickens County, SC

Contract W2 Length 12-month contract with possibilities for extension.

Benefits: Medical, Vision, Dental, Life Insurance.

Shift: Monday - Friday 5:30PM 3:30 AM

40 hours a week

Description:

Responsibilities

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 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.

Requirements

High school degree or equivalent preferred.

BEOCS

Date Added: 08-09-2022

Inside Sales Representative

19700

Colonial Heights, Virginia

Sales/Business Dev.

BEPC has an open position for an Inside Sales Representative.

Work location: Colonial Heights, VA

Contract W2 Length 6-month contract with possibilities for extension up to 24 months.

Benefits: Medical, Dental, Vision and Life Insurance

48 hours per week.

Description:

The Inside Sales Representative provides inside sales and customer support for our portfolio of Energy Conservation rebate programs. Successful candidate will be required to pass a company background check and a separate client required background prior to the start date. Company laptop provided. This is a contract position that can be extended up to 24 months. In addition, there may be a temp-to-permanent hire opportunity in the future.

RESPONSIBILITIES

• Process Energy Conservation rebate applications
• Make outbound calls to check on outstanding applications
• Uncover customer interests and needs, discuss Energy Conservation programs available
• Become a subject matter expert on our portfolio of Energy Conservation programs; promote benefits
• Discuss eligibility requirements as defined in the terms and conditions
• Resolve customer issues and address obstacles impacting the rebate process
• Drive continuous improvements in rebate processing and procedures
• Coach and train trade-ally’s (contractors) on rebate application instructions, eligibility requirements, and standard operating procedures
• Generate reports and excel spreadsheets
• Partner with program lead and field representative to resolve issues and improve performance

Basic Qualifications

• High School Degree or Equivalent
• Minimum of 5 years customer service experience
• Experience promoting program benefits
• Data entry skills (sales, orders, claims, rebates), high data entry accuracy
• Intermediate computer experience (Microsoft Word, Excel, and Outlook)

Preferred Qualifications:
• Associates or Bachelor’s degree is preferred
• Excellent written and verbal communication skills
• Ability to multi-task
• Strong Interpersonal skills; including ability to quickly establish and maintain rapport at all levels

BEPRO

Date Added: 08-09-2022

Research Associate III

19699

South San Francisco, California

Biotech/R&D/Science

Operator I

19696

Liberty, South Carolina

Manufacturing

BEPC has an open position for an Operator I

Work Location: Liberty, South Carolina.

Contract W2 Length (12 months contract with possibilities for extensions)

Benefits: Medical health, Vision, Dental, Life Insurance (25k)

Shift: 5:30PM – 03:30AM (M-F)

Category: CRM Cardiac Rhythm Management (CRM)

Full time: 40hrs/week

Description:

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.

BE OCS

Date Added: 08-09-2022

Gas and Chemical Technician

19693

Santa Clara, California

Professional

BEPC Inc. is searching for a Gas and Chemical Technician in Santa Clara, CA.

CONTRACT W2: 12 – month contract with possibilities for extensions.

** Different shifts available**

** OT available**

Job description:

Date Added: 08-09-2022

US - Buyer - G00540

19688

Clearwater, Florida

Professional

BEPC has an open position for a Buyer in Clearwater, FL!
Contract W2 Period: 6-Month contract with possibilities for extensions
Pay & Benefits: Weekly Pay +Medical, Dental, Vision and Life Insurance

Hybrid Schedule 3 days onsite/2 days remote a week.

MUST HAVE REQUIRED SKILLS:

- SAP experience
- Experience buying electronic components
- Aerospace experience
- Negotiations skills

Job Description:

Responsible for purchasing and negotiating materials, equipment, and supplies from vendors
Evaluates vendor quotes and services to determine most desirable suppliers.
Acting as a liaison between Sourcing and all other interfacing organizations to plan, coordinate and implement strategies for all Supply Chain activities related to fulfilling manufacturing and aftermarket requirements.
Heavily involved in hardware transition activities including all aspects of planning and transition execution.
Due to interface with global suppliers (time zone differences), the desirable candidate will need to be flexible on the hours worked.
Schedules, places orders and administrates purchase orders to ensure quality hardware is delivered on time.
Maintains proper inventory levels per order policy. Interacts with personnel throughout the site with frequent outside contacts to discuss/negotiate difficult technical problems.
Incumbent works under general direction with specified suppliers and hardware. Plans and schedules purchase orders in accordance with the production requirements as shown in the SAP ERP system.
Manages inventory to a specified inventory plan as required to support the production schedule.
Researches and provides constant feedback to department and management relative to material shortages and suppliers capacity and capabilities.
Demonstrates an active commitment to continuous improvement in the areas of Quality, Cost, Delivery and Lead Time.
Have effective interpersonal and communication skills with all levels of employees and management. High degree of confidence, objectivity, tact, diplomacy and ethical conduct is essential.
Demonstrated ability in negotiations, planning and hardware administration procedures
Ability to organize work, document and/or report concisely and accurately and be thorough in carrying out the responsibilities of the job.
Monitor and release kits to both internal and external suppliers to support Production and After Market needs.

Requirements

May require a bachelor's degree or 1-3 years of experience in the field or in a related area.
Knowledge of commonly used concepts, practices, and procedures within a particular field.
Relies on instructions and pre-established guidelines to perform the functions of the job.
Works under immediate supervision.
Primary job functions do not typically require exercising independent judgment.
Typically reports to a supervisor or manager.

Date Added: 08-09-2022

Operator III - 2nd Shift

19687

Temecula, California

Manufacturing

BEPC Inc is looking for an Operator I, II and III – 2nd Shift in Temecula, CA!
Contract W2 Period: 2 year contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

2^nd Shift Start time 2:00pm – 10:30pm

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
1-5+ years of experience

BEOCS

Date Added: 08-09-2022

Warehouse Operator 2

19684

Round Rock, Texas

Professional

BEPC Inc. is searching for a Warehouse Operator II in Round Rock, TX.

CONTRACT W2: 5 – month contract with possibilities for extensions.

*1^ST SHIFT 8 a.m. – 5 p.m. *

Job description:

The Logistics Specialist is responsible for proactive control of inventory within a chemical manufacturing environment. The department is responsible for storage, release, and internal and external distribution of materials following Quality and Regulatory Systems. The logistics specialist is also responsible for any International Laws pertaining to shipments. Inventory management and distribution activities impact manufacturing operations, customers, and financial transactions associated with inventory movement. These activities impact timely order fulfillment which lends to customer satisfaction and retention.

• Responsible for accuracy of inventory counts, identifying discrepancies in inventory counts and taking corrective action to guard against inconsistencies in the future.
• Receiving which includes but is not limited to matching of packing slips to purchase orders, detailed review of material, tagging and identification of material, properly storing material upon receipt, acquiring all required paperwork for receipt process, & posting inventory receipts
• Maintain up-to-date records of inventory locations
• Issuing inventory and consumable items, perform stock returns (RMA), posting of issues/returns to inventory management software,& deliver material to end user on time
• Timely management of expired and non-conforming items
• Responsible for shipment of finished goods, materials, sample, and other items in accordance with policies
• Responsible for ensuring that all shipments meet DOT and IATA regulations
• Maintain certifications required to perform job duties
• Ensure that the work areas are stocked with necessary supplies to avoid disruptions in service. Work with other personnel to maintain safety stocks for each consumable. (ie. Shippers, templates, trays, security bags etc)
• Communicate with customer service and operations regarding special shipping regulations where appropriate.
• Responsible for daily closeout of orders (posting and invoice printing)
• Responsible for ensuring adequate product stock in the distribution area
• Participate in documenting processes and identifying areas for improvement focusing on quality, efficiency, & safety.
• Maintain a safe work environment, following all company Health & Safety policies
• Perform all tasks in accordance with policies, procedures, regulatory and cGMP requirements as applicable and demonstrate capabilities through current training records.
• Proactively support activities of other areas and groups within the business

Experience and education:

High School Diploma
Experience in a chemical handling, distribution, and/or material management environment preferred.

Date Added: 08-08-2022

Associate Facilitator

19683

Not Defined

Management/Operations

Ethicon, Inc has an open position for an Associate Facilitator in San Angelo, TX!

Benefits: Medical, Dental, Vision and Life Insurance

Ethicon Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Associate Facilitator!

Ethicon, part of the Johnson & Johnson Medical Devices Companies, has made significant contributions to surgery for more than 60 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through Ethicon's surgical technologies and solutions including sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact. For more information, visit www.ethicon.com.

Are you interested in making a difference in a growing company thriving on a diverse culture, celebrating the uniqueness of our employees, and committed to inclusion? Apply today for this phenomenal opportunity!

In this role you will provide the first level of supervision in a manufacturing unit. Responsible for following all regulatory, corporate, and local policies.

Key Responsibilities:

Understands and adheres to Ethicon environmental and safety policies/guidelines, J&J Pollution Prevention Goals and regulatory requirements.
Supervises in accordance with established policies and methods to meet production commitments.
Assigns duties and actively assists, or provides direction to subordinates
Supervises work operations and employee performance.
Responsible for the safety of shift members
Works under general supervision, with responsibility to make decisions to meet operational objectives.
Erroneous decisions or recommendations or failure to get results may cause delays in program schedules and result in the allocation of additional resources.

Qualifications

Education:

A minimum of Bachelor's degree or equivalent in technical, business, logistics, engineering or related field, required

Experience and Skills:

Required:

Proficient with Microsoft systems
Excellent communication and interpersonal relation skills.
Statistical and analytical problem solving

Preferred:

A minimum 2 years of relevant work experience
Experience with JDE

Other:

Ability to travel up 10% of the time domestically
The ability to work overtime, off-shift hours and some holidays as needed by business is required.

At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love. As such, candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.]

Date Added: 08-08-2022

Electrician

19682

Not Defined

Technical

Ethicon Inc., member of Johnson & Johnson’s Family of Companies is currently recruiting for Electrician, located in San Angelo, TX.

Full time, direct hire with competitive pay!

Company Description:

Ethicon offers a broad range of products, platforms, and technologies—including sutures, surgical staplers, clip appliers, trocars, and synthetic mesh devices—that are used in a wide variety of minimally invasive and open surgical procedures. Specialties include support for treatment of colorectal and thoracic conditions, women’s health conditions, hernias, cancer, and obesity. Ethicon Endo-Surgery, Inc. was created 20 years ago in Cincinnati, Ohio, developing innovative devices that have driven the revolutionary shift from open to minimally invasive surgery that continues to lead the industry today.

Job Summary

Electricians are expected to work on all electrical and electronic equipment, such as electrical components, controllers, programmable logic controllers, electric motors, control panels, instrumentation device, wire, cables, printers, conduit, etc. In addition to all electrical and electronic tasks, Electricians are responsible for recording and maintenance of all critical data and documentation. This position focuses on continuous improvement and maximum efficiency from the machinery, ensuring maximum machine utilization, and minimum departmental non-production time.

Duties & Responsibilities:

Under general supervision and in accordance to prescribed procedures and requirements performs complete electrical and electronic maintenance support including but not limited to installation, diagnosis, troubleshooting, adjustments, repair, preventive and emergency maintenance as well as continuous improvement. Electricians are expected to work on all electrical and electronic equipment, such as electrical components, controllers, programmable logic controllers, electric motors, control panels, instrumentation device, wire, cables, printers, conduit, etc. In addition to all electrical and electronic tasks, Electricians are responsible for recording and maintenance of all critical data and documentation. This position focuses on continuous improvement and maximum efficiency from the machinery, ensuring maximum machine utilization, and minimum departmental non-production time.

Duties & Responsibility include:

Must read, interpret and follow work instructions and training materials.
Pass and maintain training and certification examinations as required.
Read diagrams, sketches, blueprints, diagrams, operation manuals and manufacturing specifications related to assigned equipment.
Use process controller programmer systems to maintain programs and to diagnose equipment failures using analysis of relay-ladder-logic programs and other process control language software.
Diagnose and identify equipment failures within entire the system which may not be electrical in nature, e.g., mechanical, pneumatic, or facilities.
As required, maintain area support equipment, e.g., electrical utilities, lights, etc.
Operates all portable power tools and hand tools in assigned production area; drills, wrenches, grinders and meters to troubleshoot and repair of production equipment.
Accurate record keeping via computer management systems and/or via manual systems by inputting and retrieving maintenance data, and other pertinent data following standard procedures. Assure that all maintenance work performed on said equipment and spare parts used are captured in CMMS.

Responsible for interpreting computer based diagnostic data for predictive maintenance and other applications.
Electricians are accountable to utilize trade knowledge and familiarity with plant and equipment for leading a continuous improvement program on specified equipment. This will include recommending, and participating in equipment improvements, PM process improvements, and OEE tracking/trending.
Work as member of the Ethicon Performance Excellence (EPS), Manufacturing Equipment Excellence (ME2), or LEAN team to achieve specific goals.
Follow current compliance regulations and standards.
Perform all work in accordance with ISO 14001 principles and environmental regulatory compliance requirements, within safety requirements inherent to chemical process and high voltage electrical work and within all safety codes, including but not limited to NFPA, NEC, applicable building and with engineering on material and operation acceptability of all parts used inside classified hazardous areas. Electrical repairs or modifications that impact personal or process safety must be reviewed by the Safety Audit Team prior to implementation.
Independently recognize and solve problems with the ability to make critical decisions under pressure on breakdowns and works towards effectively managing deadlines in completing breakdown, maintenance and project activities. safety codes, ETHICON requirements, etc. Work within engineering safety guidelines, checking
Associates holding this position will always demonstrate the ability to work with, and communicate well with others, ability to give and understand instructions, both verbal and written. Coordinate, instruct, advise, and train other craft personnel as needed.
Maintains general housekeeping within the department, keeping equipment and work area clean and orderly. Maintain inventory of spare parts and notify supervisor when parts are needed.
Does any other work of a related nature and performs other work related duties as assigned.
Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001).

Tech 1 – (Class C – Job Level C-3)

Must understand and demonstrate comprehension of the following but not limited to:

Operates all portable power tools and hand tools in assigned production area; drills, wrenches, grinders and meters to troubleshoot and repair of production equipment.
Performs routine and scheduled maintenance to production equipment.
Possesses electromechanical knowledge to be used in problem diagnosis and solutions.
Possesses a basic understanding of the use of electrical schematics for the purpose of troubleshooting and repair.
Works towards effectively managing deadlines in completing breakdown, maintenance and project activities.
Ability to make critical decisions under pressure on breakdowns.
Perform and document electrical related PM’s (Planned Maintenance) on process equipment as assigned.
Document all equipment service activities and modifications in the process Equipment Logbook as well as CMMS.

Qualifications

REQUIRED EXPERIENCES AND QUALIFICATIONS:

- High school diploma, G.E.D. or equivalent skills, experience, or training.
- Generally, Requires 0-2 Years Work Experience
Computer knowledge in Microsoft Office including EXCEL, WORD, and Outlook and able to demonstrate the ability to operate Microsoft Excel for data entry and interpretation (Open selected files given location, read and interpret data as displayed, tabular and graphically).
Knowledge of PLCs and automated equipment is preferred

At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love. As such, depending on location and subject to local legislation, candidates offered employment may be required to show proof of COVID-19 vaccination or, in certain countries, secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work. If you are invited to interview for the position, your recruiter will advise on the vaccine requirement status in your geographic location.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

BEPRO

Date Added: 08-08-2022

Senior Asset Reliability Management Engineer

19681

Not Defined

Engineering

BEPC Inc. searching for a person to be
A DIRECT HIRE.

Urgent need for a STABLE and long employment relation.

Job Description

Ethicon, a member of Johnson & Johnson Family of Companies, is recruiting for a Senior Asset Management Engineer located in San Angelo, TX

The Ethicon business offers a broad range of products, platforms and technologies-including sutures, topical skin adhesives, hemostasis products, surgical staplers, trocars, energy devices and synthetic mesh devices-used in a wide variety of open and minimally invasive surgical procedures. Specialties include orthopedics, support for treatment of colorectal and thoracic conditions, women's health conditions, hernias, cancer and obesity. The Ethicon business combines products and services of two market leading legacy companies, both with long histories of medical innovation. Ethicon, Inc. based in Somerville, New Jersey, was founded more than 80 years ago as a pioneer in suture development and manufacturing, helping to transform the safety and effectiveness of surgery. Ethicon Endo-Surgery, Inc., based in Cincinnati, Ohio, was founded 20 years ago to develop innovative devices that have driven the groundbreaking shift from open to minimally invasive surgery that continues to lead the industry today.

The Senior Asset Management Engineer will be responsible for the engineering and quality assurance a part of a major project or for a complete small project. Reviews and analyzes complex task statements, standards, specifications, engineering drawings and other documentation to determine engineering requirements. May direct preparation of milestone charts, manpower and material estimate inputs, and related material needed to define program schedules and Prepares reports, proposals, and presentations. Analyzes customer technical requirements and recommends solutions beneficial to the customer and to the company's engineering and scientific reputation. Responsible for assuring that the generation, release, and maintenance of documentation is in accordance. Designs complex mechanical, electronic, and electrical assemblies and systems using typical components.

Key Responsibilities:

Lead the Site Reliability journey
Lead reliability studies and analysis to conduct root cause/problem solving analysis of reliability problems on automated equipment
Determine, lead, and execute action plans that will lead to improve reliability and performance/Overall Equipment Effective (OEE) of manufacturing equipment
Create/lead Failure Modes and Effects Analysis (FMEA), Failure Modes and Effects Criticality Analysis (FMECA), reliability hazard analysis, predictive and preventive maintenance, accelerated testing techniques, and application of statistical analysis
Translate relevant data/information into broadly understandable terms to convey risks and provide the means by which project trade off discussions and decisions may be made
Participate in design for reliability efforts and reviews
Ensure effective and efficient use of Process Excellence tools (Six Sigma/Lean Manufacturing) and techniques to solve reliability opportunities
Evaluate and improve Preventive Maintenance program
Develop/improve Preventive Maintenance job plans through reliability methodology
Evaluate and improve spare part management and inventory
Identify and lead projects that deliver cost reduction of maintenance program
Evaluate technical skills (skills gap assessment) of Maintenance team (Electricians and Mechanics) and develop/execute training and development program
Perform/support troubleshooting of manufacturing equipment (high speed automation)
Perform/execute process and equipment modifications and validations
Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001)

Qualifications

Education:

Bachelor’s Degree required; B.S in engineering is preferred
Lean or Six Sigma (Green or Black Belt) Certification preferred

Required:

Minimum of four (4) years of relevant work experience in a manufacturing environment
A minimum of 2 years of Maintenance/Reliability experience
Experience with technical documentation writing
Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook)
The ability to collaborate with all levels of management and influence decision-making in a cross-functional team environment

Preferred:

Experience in the manufacturing of Medical Devices
Experience with automated equipment: Programmable Logic Controllers (PLCs), Vision Systems, Computer Integrated Manufacturing (CIM), Robotics
Experience with design of equipment
Experience with packaging or sterilization processes
Experience with skills development/improvement programs for maintenance personnel
Knowledge in Maintenance and Reliability programs and applicable tools
Process validation experience
Knowledge of Quality Systems (e.g. CAPA, NCR)

At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through innovative programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love. As such, candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

Date Added: 08-08-2022

Senior Equipment Engineer

19680

Not Defined

Engineering

Ethicon, a member of Johnson & Johnson Family of Companies, is recruiting for a Senior Equipment Engineer located in San Angelo, TX

Full time, direct hire with competitive pay!!!

The Senior Equipment Engineer will apply comprehensive and diverse knowledge of engineering principles and practices within broad assignment areas and coordinate and direct activities of technical support staff (salary and wage) and will be responsible for technical development of assigned staff. Responsible for Providing Subject Matter Expertise and Platform Ownership on multiple equipment types and technologies, including equipment reliability.

Key Responsibilities:

Plan, conduct and direct engineering projects or studies, including complete projects requiring advanced knowledge of a specialized field.
Apply comprehensive and diverse knowledge of engineering principles and practices within broad assignment areas.
Coordinate and direct activities of technical support staff (salary and wage) and will be responsible for technical development of assigned staff.
Track and trend data, identify and implement process improvements to improve business measures.
Investigate product inquiries, develop and implement appropriate corrective actions.
Provide Subject Matter Expertise and Platform Ownership on multiple equipment types and technologies, including equipment reliability.
Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001). This includes, but is not limited to, validation documents, NCR/CAPA/Internal audit investigations, Validation Master Plan (VMP) activities and any other applicable quality system task.
Performs other duties assigned by supervisor/manager as needed.

Qualifications

Education:

Bachelor’s Degree required; B.S in engineering or a related technical discipline
A Master's degree or PhD in Engineering preferred.
Lean or Six Sigma (Green or Black Belt) Certification preferred

Required:

Minimum of four (4) years of relevant work experience in a manufacturing environment
Experience with technical documentation writing
Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook)
Must have strong analytical problem-solving skills and professional judgment required to resolve major technical issues.
The ability to collaborate with all levels of management and influence decision-making in a cross-functional team environment

Preferred:

Experience on packaging processes and equipment
Medical Device, Consumer or Pharmaceutical industry experience
Experience with Programmable Logic Controllers (PLCs) (i.e. programming, writing code, etc.)
Experience with vision systems, Robotics and automation
Experience with Computer Integrated Manufacturing (CIM)
Experience with high-speed automation assembly equipment
Knowledge of FDA, ISO and/or GMP regulatory requirements
Knowledge of BSI (European) regulatory requirement
Project management experience
Must be capable of making effective management level presentations, writing formal reports dealing with both technical and business implications, and preparing project plans.

Other:

This position will require up to 10% travel.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

Date Added: 08-08-2022

Base Business Engineer

19679

Not Defined

Engineering

Ethicon, Inc has an open position for a Base Business Engineer in San Angelo, TX!!
Benefits-Medical, Dental, Vision and Life Insurance

Ethicon Inc., member of Johnson & Johnson’s Family of Companies is currently recruiting for Base Business Engineer, located in San Angelo, TX.

Company Description:

Job Summary

Makes decisions regarding engineering problems and methods and represents the company in conferences to solve problems and to plan and coordinate work. Under limited supervision, support and lead craft associates with equipment issues. Responsible for the engineering and quality assurance of part of a major project or for a complete small project. Reviews and analyzes complex task statements, standards, specifications, engineering drawings and other documentation to determine engineering requirements. May direct preparation of milestone charts, manpower and material estimate inputs, and related material needed to define program schedules. Prepares reports, proposals, and presentations. Analyzes customer technical requirements and recommends solutions beneficial to the customer and to the company's engineering and scientific reputation. Responsible for assuring that the generation, release, and maintenance of documentation is in accordance. Provides technical expertise and assistance to assigned engineers, drafters, and technicians. Analyzes test data for accuracy and consistency. May inspect, certify, and evaluate onsite operational systems an establishes test plans and guides technicians in the collection of test data in a form suitable for analysis. Determines appropriate test criteria and procedures and analyzes data comparing against specified and computed values, making changes and improvements where needed. Plans and conducts work requiring judgment in the independent evaluation, selection and substantial adaptation and modify

Duties & Responsibilities:

Lead reliability studies and analysis to conduct root cause/problem solving analysis of reliability problems on automated equipment.
Determine, lead, and execute action plans that will lead to improve reliability and performance/Overall Equipment Effective (OEE) of manufacturing equipment.
Create/lead Failure Modes and Effects Analysis (FMEA), Failure Modes and Effects Criticality Analysis (FMECA), reliability hazard analysis, predictive and preventive maintenance, accelerated testing techniques, and application of statistical analysis.
Translate relevant data/information into broadly understandable terms to convey risks and provide the means by which project trade off discussions and decisions may be made.
Participate in design for reliability efforts and reviews.
Ensure effective and efficient use of Process Excellence tools (Six Sigma/Lean Manufacturing) and techniques to solve reliability opportunities.
Evaluate and improve Preventive Maintenance program.
Develop/improve Preventive Maintenance job plans through reliability methodology.
Evaluate and improve spare part management and inventory.
Identify and lead projects that deliver cost reduction of maintenance program.
Evaluate technical skills (skills gap assessment) of Maintenance team (Electricians and Mechanics) and develop/execute training and development program.
Perform/support troubleshooting of manufacturing equipment (high speed automation).
Perform/execute process and equipment modifications and validations.
Lead craft associates when required. Assign task and resources depending on current production priorities.
Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001).

Qualifications

REQUIRED EXPERIENCES AND QUALIFICATIONS:

A minimum of 2 years of experience in the manufacturing of Medical Devices is preferred.
A minimum of 2 years of Maintenance/Reliability experience is preferred.
Experience with one or more of the following is preferred: Programmable Logic Controllers (PLCs), Vision Systems, Computer Integrated Manufacturing (CIM), Robotics.
Experience with automated equipment is preferred
Experience with design of equipment is preferred.
Experience with packaging or sterilization processes preferred.
Experience with technical documentation writing is required.
Experience in mentoring/coaching is preferred.
Experience with skills development/improvement programs for maintenance personnel is preferred.
Knowledge in Maintenance and Reliability programs and applicable tools preferred.
Process validation experience is preferred.
Mechanical and electrical skills preferred.
Knowledge of Operational Equipment Effectiveness (OEE) is preferred.
Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is required.
Knowledge of statistical data analysis tools (e.g. Minitab) preferred.
Knowledge of FDA, ISO and GMP regulatory requirements required.
Knowledge of Process Excellence (Lean, Six Sigma) tools and methodologies preferred.
Lean or Six Sigma (Green or Black Belt) Certification is preferred.
Must have excellent communication skills.
Must be organized, detail-oriented, and results/performance driven.
The ability to collaborate with all levels of management and influence decision-making in a cross-functional team environment is required.

At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love. As such, depending on location and subject to local legislation, candidates offered employment may be required to show proof of COVID-19 vaccination or, in certain countries, secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work. If you are invited to interview for the position, your recruiter will advise on the vaccine requirement status in your geographic location.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.

Date Added: 08-08-2022

Compliance Engineer

19678

Not Defined

Engineering

BEPC Inc.
Searching for a qualified Candidate

Compliance Engineer to be located in San Angelo, TX

Ethicon, part of the Johnson & Johnson Medical Devices Companies, has made significant contributions to surgery for more than 60 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through Ethicon's surgical technologies and solutions including sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact. For more information, visit www.ethicon.com.

The Regulatory Compliance Engineer II conducts assignments encompassing complete projects or portions of major projects. They determine methods and techniques to be used or adapt standard methods to meet variations. They coordinate phases of work internally and externally. In addition to those activities pertaining to the Associate level of the position, the Regulatory Compliance Engineer II also oversees responsibilities related to external audit/inspection readiness, data trending, system support, audit planning and audit program management.

Compliance Engineer Duties & Responsibilities:

External Audit/Inspection Readiness and Management:

Support external audit/inspection readiness activities to ensure site readiness at all times including audit logistics, from room/backroom arrangements, identifying/preparing SME’s, etc.
Support external audits/inspections of the site e.g. Notified Body, Health Authority, Ministry of Health, FDA, Regulatory Agency, or JJRC/ERC.
As required, assess the risk and applicability of external audit/inspection observations from other J&J facilities to determine impact to the site.
Support mock external audits/inspections as part of External Audit/Inspection Readiness activities.
Provide timely information to support the external audit/inspection process.
Provide guidance to prepare responses to any regulatory agency notification or correspondence associated with the site.
Provide guidance to ensure timely and adequate responses to external audit/inspection observations related to the site, including failure investigations, root cause analysis, risk assessments, correction, corrective and preventive action plans, monitor and drive on-time completion of all action plans, perform follow-up with owners, and perform effectiveness monitoring and closure.
Ensure timely and accurate reporting and publishing of external audit metrics. Drive compliance and improvements in metrics targets.

Internal Audit Program and Management Execution:

Execute internal audits according to the established internal audit procedures.
Ensure internal audit results are reported to management having responsibility for the matters audited.
Ensure timely and adequate responses to internal audit observations, including failure investigations, root cause analysis, risk assessments, correction, corrective and preventive action plans, monitor and drive on-time completion of all action plans, perform follow-up with owners, and perform effectiveness monitoring and closure
Ensure timely and accurate reporting and publishing of internal audit metrics. Drive compliance and improvements in metrics targets.
Ensure documentation and records related to the internal audit program are maintained.
Ensure all quality system elements/processes applicable to the site are audited and appropriate actions are taken to meet the business and regulatory requirements.

Enterprise, Sector and JJRC Support:

Participate in JJRC audits as requested.
Connect and collaborate with the compliance teams of other sites, regions and business groups.

Metrics Collection and Reporting:

Assure that internal and external audit metrics are consistently and accurately captured, and that they are reported and published at the appropriate level for subsequent analysis and reporting (e.g., site level, supply chain).
Drive compliance and improvements in metrics targets.
Create reports and communicate performance against metrics to key stakeholders.
Highlight/communicate adverse trends in metrics and take risk-based action to remediate.

Escalations:

Escalate quality issues in accordance with established procedures.

External Standards and Regulations:

Support implementation of new/revised regulations and standards for the site.
Maintain current knowledge of regulatory changes through industry publications, seminars, professional affiliations, and industry meetings.

Site Management Review and Data Review Board (DRB):

Provide input into Site Management Reviews and Data Review Boards (e.g., internal audits.) to allow meaningful reviews.

Other Tasks:

Establish strong connection and collaboration with business partners at the site, e.g. Quality Operations, Training, and Manufacturing.
Provide/coordinate regulatory compliance education and training (QSR, ISO, GMPs) to the organization in support of overall educational/training strategies.
Perform performance appraisals and establish goals/objectives and development plans for direct reports.
Comply with all environmental, safety and occupational health policies and ensure all direct reports comply with those requirements
Comply and ensure compliance of employees under area of responsibility with the Quality System regulations, standards, company policies and procedures.

At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional, and financial health of our employees and the ones they love. As such, depending on location and subject to local legislation, candidates offered employment may be required to show proof of COVID-19 vaccination or, in certain countries, secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work. If you are invited to interview for the position, your recruiter will advise on the vaccine requirement status in your geographic location

Qualifications

Bachelor of Science degree is required
Written Communications skills required
Degree in technical area preferred
Experience in the FDA/ISO/Health Authority-regulated industry (medical devices or pharmaceutical), regulated medical device operation preferred
2-4 years’ experience in Quality, Manufacturing or Engineering roles is preferred.
Auditing experience is preferred.

BEPC Inc.

???????325-315-2180

Date Added: 08-08-2022

Material Handler

19676

Des Plaines, Illinois

Manufacturing

BEPC has an open position for a Material Handler

Work Location: Des Plaines, Illinois

Contract W2 Length (4-month contract with possibilities for extensions)

Benefits: Medical health, Vision, Dental, Life Insurance (25k)

Shift: 07:00AM – 4:00PM (M-F)

Category: Heavy Industrial

Description:

Job Summary: Briefly state the main purpose and scope of the job. The Material Handler II is responsible for ensuring all inventory is maintained accurately and provided to required areas in a timely manner.

Job Duties:

Tasks or responsibilities which employees in this position are required to perform.
Perform Material Movements both physically and systematically
Generate Work Orders from an ERP system
Perform Work Order Receipts in ERP system
Perform cycle counting as required
Maintain a neat and safe work environment
Assist in the coordination and flow of product through manufacturing and assembly when needed
Work in a cross functional team environment
Some areas will require the handling of chemicals with proper training provided
May required to work overtime as required for business needs
Support 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, 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.
Performs other related duties and responsibilities, on occasion, as assigned.
Prefer SAP experience

BEOCS

Date Added: 08-08-2022

Production Tech

19675

Scottsdale, Arizona

Manufacturing

Operator I

19674

Irvine, California

Manufacturing

BEPC Inc. is actively looking for a Operator for the 1^st shift in the Irvine, California area. 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.

EDUCATION: High school diploma or GED

LOCATION: On Site

DUTIES/RESPONSIBILITIES:

- 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.

BEOCS

Date Added: 08-08-2022

Warehouse Operator 2

19673

Round Rock, Texas

Professional

BEPC Inc. is searching for a Warehouse Operator II in Round Rock, TX.

CONTRACT W2: 5 – month contract with possibilities for extensions.

*1^ST SHIFT 8 a.m. – 5 p.m. *

Job description:

Experience and education:

High School Diploma
Experience in a chemical handling, distribution, and/or material management environment preferred.

Date Added: 08-08-2022

Contracts Manager

19671

Newark, New Jersey

Legal

BEPC is seeking a skilled Contracts Manager 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!

ABOUT THIS ROLE
We are seeking a bright and motivated Contracts Manager to support our growing original content initiatives. You will be client-service oriented, have great attention to detail while still meeting tight deadlines, have great organizational skills, and have the ability to easily switch gears. A high level of integrity and discretion in handling confidential information and professionalism in dealing with senior professionals inside and outside the company is essential.

ABOUT YOU
You have the uncanny ability to know where you are needed, identify and implement process improvements, effectively manage internal and external relationships, and work cross-functionally with other teams. You are able to handle a high volume of tasks and projects independently, react with appropriate urgency to situations and events that require a quick response or turnaround, take effective action without having to know the total picture, and solve problems that affect a broad range of teams.

As a Contracts Manager, you will...

Review, draft and negotiate a variety of content acquisition, development, and production-related agreements in connection with original audio content.
Set up and maintain rights management systems for our content slate.
Oversee and manage a wide range of content production-related workstreams involving third-party production companies, talent and other creative contributors.
Develop self-service legal tools and train business units on best practices relating to self-service legal tools.
Maintain business-facing resources. Update and maintain repository of agreement forms and terms.
Prepare agreements for signature.
Assist with other tasks and projects on an as-needed basis.

Basic qualifications

3+ years of paralegal, contracts manager, rights clearance, or other comparable experience including experience in the entertainment, media, technology and/or publishing fields.
Bachelor’s or Associate’s Degree.

Preferred qualifications

Previous in-house legal experience.
Strong written and verbal communication skills.
Working knowledge of legal concepts related to contracting, licensing, and content production, including copyright and trademark law.
Capacity to function autonomously yet communicate laterally and upwardly with ease.
Exceptional interpersonal skills to effectively coordinate complex issues and projects with diverse levels of management and employees.

BEPRO

Date Added: 08-08-2022

Principal Scientific Researcher - Oncology Biomarker

19666

South San Francisco, California

Biotech/R&D/Science

BEPC Inc. has a great job opportunity for a Principal Scientific Researcher in South San Francisco, CA!

W2 Contract for 5 months with opportunity for extensions.
Weekly pay and benefits: Medical, Dental, Vision and Life Insurance.

Job description:

The Department of Oncology Biomarker Development (OBD) is seeking a highly motivated independent laboratory based Principal Scientific Researcher/Senior Scientific Researcher to contribute to translational research with the goal of identifying and validating novel mechanisms of response and resistance to oncogene targeted therapies in support of early and late-stage assets.

Essential duties and responsibilities:

Specific responsibilities will include working closely with his/her supervisor, carrying on highly independent research to build scientific hypothesis, design/execute experiments, collaborate with colleagues across multifunctional groups, data analysis, and presenting findings to teams.
Experimental strategies will include the application of state of the art molecular and genomic/epigenomic technologies to analyze pre-clinical and clinical samples
Other job relevant tasks include multitasking, organization, record keeping, problem solving with good time management skills, and contributions to publications.

Requirements:

Successful candidates will have BA/BS or MS with 5+ years of experience (Senior Scientific Researcher) or BA/BS or MS with 8+ years of experience or PhD with several years of hands-on laboratory research experience with successful completion of a post-doctoral study (Principal Scientific Researcher) in Cancer Biology, Cell Biology, Molecular Biology, or Biochemistry.
The candidates should be committed to doing bench work and demonstrate strong passion on translational cancer research to present work to wide scientific audience.
The candidates will have an intimate knowledge of, and extensive hands-on experience with, relevant molecular (e.g., PCR, DNA manipulation), cell biology techniques (e.g. primary and derivative cell culture), and Biochemistry (e.g. SDS-PAGE, Western blotting, Protein assays, Enzyme assays).
Preferred candidates will have experience in oncology, especially in oncogene-mediated signaling cascade.
Experience in multi-omics, single cell sequencing and bioinformatic skill is desired but not required.
Candidates must have good communication skills and the ability to work with scientists and associates from multiple laboratories, disciplines, and departments.
Candidates will have a proven publication track record for productivity and technical independence.

BEOCS

Date Added: 08-08-2022

Scientific Researcher

19665

South San Francisco, California

Biotech/R&D/Science

BEPC has an open position for a Scientific Researcher!

Location: South San Francisco, CA
Requisition ID: ROCGJP00018826
Contract W2 length: 1 year contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Duties:

The Clinical Pharmacology (CP) Scientific Researcher is responsible for the delivery of PK/PD analyses and reports for their assigned development project[s], in order to ensure that appropriate dose/route/schedule decisions are made for the patients. The CP Scientific Researcher typically works under the supervision of a CP Scientist, in order to deliver the PK/PD elements of the agreed CP strategy. The CP Scientific Researcher works closely with colleagues in data programming, biostatistics and or infrastructure to facilitate the timely preparation and transfer of data sets containing PK/PD and critical patient demographic and treatment data for analyses. Performs other duties as assigned.

Technical Skills:

Familiarity with quantitative approaches in drug development, working knowledge of or a strong desire and ability to learn data programming tools (eg. NONMEM, WinNonlin, Berkeley Madonna, R, S-Plus, SimCYP, GastroPlus) and the ability to plan, organize and perform PK/PD data analyses.
Working knowledge of statistical approaches as they apply to clinical study design & analysis.
Working knowledge of relevant disease areas.

Communication Skills:

The CP Scientific Researcher requires strong communication skills, both written and oral, in order to deliver high quality protocols, regulatory documents, documents for team and management review, scientific manuscripts & posters for publication.

Drug Development Knowledge:

The CP Scientific Researcher should have a good knowledge of GCP and working knowledge of relevant regulatory guidelines.

Leadership:

Based on experience and ability, the CP Scientific Researcher may lead CP teams, project sub-teams and represent CP at cross-functional project teams.

Qualifications:

BA or BS in Statistics, Mathematics, Biology, Chemistry, Pharmaceutical Sciences, Biomedical Engineering, or related quantitative discipline is required

BEOCS

Date Added: 08-08-2022

Processing Operator I

19661

Altavista, Virginia

Manufacturing

Sr Engineering Support Specialist

19660

Clearwater, Florida

Engineering

Sr Engineering Support Specialist

19659

Tempe, Arizona

Engineering

BEPC has an open position for a SR Engineering Support Specialist in Tempe, AZ!

Contract W2 Period: 6-month contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Complete review of suppliers' certification packages and creation of logbooks for Space, Missile, and Marine customer hardware to support completion of customer deliverables. The following tasks aid in driving success:
• Obtain and analyze drawings/blueprints, specifications, other technical source data, customer and supplier purchase orders, etc., to determine that supplier certification and FAIR packets meet program requirements, including all customer flow down
• Coordinates/interfaces with program personnel, including but not limited to Program Management Project Engineering, Quality, Purchasing, Contracts, Configuration Management, etc.
• Identifies, processes, records, maintains, retrieves, and compiles contractual data for submittal to the customer in accordance with contractual requirements
• Prepare logbooks per customer requirements
• May support pre-ship reviews and drive closure of action items as required
• Plans, organizes, and participates in logbook and certification audits
• Maintains positive supplier and customer relationships through open communication and regular interaction
• Prepares and implements data management plans and status reports for assigned programs
• Responsible for process evaluation, control, and continuous improvement in all data management activities
• Responsible for scheduling all work through the area and executing to the planned schedule
• This position is located in Tempe, Arizona
Basic Qualification:
• 3+ years' experience in Data management, Quality, or equivalent

Additional Qualifications:
• Knowledge of ISO 9001 and AS 9100 manufacturing standards
• Excellent communication and problem-solving skills, Presentation skills, Detail-oriented, self-managing, motivated, must exercise initiative
• Capable of reading and understanding blueprints and other technical documents
• Auditing experience
• Experience managing external suppliers
• Six Sigma knowledge and experience
• Experience Building strong customer relationships and resolving problems, Coordinating and scheduling the work activities of a team is desired
• Creation of BOM and Parts lists Attribute/Skills Sought Supply Chain or Quality Background
• Experience with Missile Valve Product Knowledge and Managing data on a complex program
• Experience working on Military or government contracts, Implementing process improvements and SAP applications

BEOCS

Date Added: 08-08-2022

Principal Software Engineer

19658

Minneapolis, Minnesota

Engineering

BEPC has an open position for a Principal Software Engineer in Minneapolis, MN!
Contract W2 Period: 6-month contract with possibilities for extensions
Pay & Benefits: Weekly pay. +Medical, Dental, Vision and Life Insurance

Description:

ONSITE ONLY.

Leading the full lifecycle develop of embedded real time safety critical navigational software. These solutions are defined from requirements, implemented in code, verified in simulation & hardware testing, and certified with government and safety organizations as part of Companys Aerospace Products.
• Requirements decomposition and work assignments
• Sensor management & navigational feature definition & design
• Software architecture and coding of Realtime OS
• Integration & System activities
• Certification & Artifacts
• Unit Test & coordination of External Verification & Validation activities
• Factory deployment and support
• Ability to code in multiple languages

YOU MUST HAVE
• Bachelor’s degree in Engineering, Computer Science, Mathematics, or Physics
• 7+yrs of quantified experience in software engineering using C/C++
• 5+yrs of quantified experience in DO-178 B/C development & artifact generation, or equivalent high-rigor processes

WE VALUE
• Understanding various software development lifecycle (waterfall, Agile)
• Demonstrate the ability to develop efficient and high-quality embedded software and architecture
§ DDC-I DeOS operating system
§ Inertial Sensor or Commercial Navigation experience
§ GPS
• Developed software in certified or regulated safety environments (C/C++)
• Knowledge of software configuration management and change management practices
§ GIT / BitBucket
§ Jira
• Diverse and global teaming and collaboration
• Effective communicator
• Team leadership and coordination experience
• Can quickly analyze, incorporate, and apply new information and concepts
• Ability to consistently make timely decisions even in the face of complexity, balancing

Be pro

Date Added: 08-08-2022

US - Sr Advanced Mechanical Engineer

19656

Torrance, California

Engineering

Sr Engineering Support Specialist

19654

Phoenix, Arizona

Engineering

Sr Electrical Technician

19653

Phoenix, Arizona

Technical

Sr Advanced Software Engineer

19652

Clearwater, Florida

Engineering

BEPC has an open position for a Sr Advanced Software Engineer in Clearwater, FL!
Contract W2 Period: 6-month contract with possibilities for extensions
Pay & Benefits: Weekly Pay +Medical, Dental, Vision and Life Insurance

Description:

REMOTE ROLE

Leading the full lifecycle develop of embedded real time safety critical navigational software. These solutions are defined from requirements, implemented in code, verified in simulation & hardware testing, and certified with government and safety organizations as part of Company’s Aerospace Products.
• Requirements decomposition and work assignments
• Sensor management & navigational feature definition & design
• Software architecture and coding of Realtime OS
• Integration & System activities
• Certification & Artifacts
• Unit Test & coordination of External Verification & Validation activities
• Factory deployment and support
• Ability to code in multiple languages

YOU MUST HAVE
• Bachelor’s degree in Engineering, Computer Science, Mathematics, or Physics
• 7+yrs of quantified experience in software engineering using Matlab / Simulink

WE VALUE
• Understanding various software development lifecycle (waterfall, Agile)
• Demonstrate the ability to develop efficient and high-quality embedded software and architecture derived from Matlab & Simulink design
§ GPS (SASSM or M-Code) operation
§ Modeling approaches
• Knowledge of software configuration management and change management practices
§ DOORS
§ GIT / BitBucket
§ Jira
• Diverse and global teaming and collaboration
• Effective communicator
• Team leadership and coordination experience
• Can quickly analyze, incorporate, and apply new information and concepts
• Ability to consistently make timely decisions even in the face of complexity, balancing systematic analysis with decisiveness
• Ability to convey subtle or complex messages clearly, as appropriate for the topic and audience

Be Pro

Date Added: 08-08-2022

Sr Mechanical Design Engineer

19648

Phoenix, Arizona

Engineering

BEPC is seeking 5 skilled and talented Sr Mechanical Design Engineers 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!

This is an exciting and challenging opportunity to use advanced mechanical design expertise on complex components for aerospace gas turbine engines and power generation systems. The focus of this role is gearbox design which includes layout and design of the internal components and housings. The mechanical designer may also design core internal components of gas turbine engines. The primary functions are to create 2D drawings and 3D CAD models using Siemens NX and Teamcenter. Experience with FEA and topological optimization tools is desired to ensure weight-optimized designs. Interact closely with project engineers and design teams meet project deliverables and milestones. Understand and adhere to Geometric Dimensioning & Tolerancing practices, act with speed and accuracy for on-time execution and apply six sigma thought processes and tools. Listen to internal customer’s needs and support team in reducing cycle time and improving quality of deliverables.

Preferred Qualifications:

Proficiently create, revise, and validate 3D CAD models and 2D drawings using NX and Teamcenter.
Experience in gearbox layout and design, and internal gas turbine engine components.
Demonstrate an advanced understanding of Geometric Dimensioning and Tolerancing.
Possess a thorough understanding of applicable design manuals and best practices.
Ability to understand issues with legacy models, drawings, and casting tooling and effectively communicate problems and present solutions.
Effectively conduct design reviews and complete action items in timely manner.
Strong organizational skills are needed to help keep track of multiple tasks and priorities.
Proficient technical report writing and presentation skills.
Effective interpersonal and team skills to resolve problems and to improve engineering-manufacturing integration.
Mindset to improve processes and reduce cycle time.

You Must Have:

Bachelor of Science in Mechanical or Aerospace Engineering
CAD Design 4 Years Minimum

BEPRO

Date Added: 08-05-2022

Engineer, Quality

19647

Temecula, California

Manufacturing

MRO Buyer/Planner

19646

South San Francisco, California

Purchasing/Supply Chain

BEPC Inc. has a great job opportunity for an MRO Buyer/Planner in South San Francisco, CA!

W2 Contract for 16 months with opportunity for extensions.
Weekly pay and benefits: Medical, Dental, Vision and Life Insurance.

Job description:

Responsible for understanding all areas of the business rules involving order processing, inventory, purchasing, Material Requirements Planning (MRP), and related accounting impacts to operations.

Works closely with other Buyers, Inventory Analyst, & Receiving to maintain adequate inventory levels and customer satisfaction.

Essential duties and responsibilities:

Initiates RFQ’s (request for quotes) process daily and as assigned. Manage timely receipt of quotes from vendors. Update requisitions with delivery dates/lead times, and relevant notes or blocking comments; information necessary to communicate status of material.
Sources materials from a list of preferred vendors.
Develop and maintain vendor relationships.
Update purchasing info records related to sourcing activities.
Processes POs (Purchase Order) in a timely manner and obtain PO acknowledgements from Suppliers.
Update POs with delivery dates/lead times, and relevant notes necessary to communicate status of material.
Monitors open purchase orders for all orders to ensure on-time deliveries (OTD), alert Storeroom, Planning, and/or management as needed of any potential issues.
Utilizes MRP System to procure materials consistent with quality and delivery expectations.
Tracks in-transit material as required identifying and addressing any potential delivery issues.
Reviews and execute Return-to-Vendor requests as required.
Manage process to ensure credit memos or replacement materials are received.
Addresses invoice resolution activities in a timely manner related to blocked/parked invoices.
Timely resolution of POs in blocked status “problem POs”.
Review and resolve non-conformances, packing slip and certificate of compliance issues in a timely manner.
Resolution with internal partners and external suppliers required.
Communicates/escalates any engineering or quality changes observed to vendors and the company’s groups for evaluation.
Submits technical support “Tech Support” requests as required when master data discrepancies are identified.
Helps manage and communicate vendor performance to ensure on time deliveries and adherence to quality specifications.

Desired skills:

Demonstrate knowledge of standard concepts and practices in Purchasing.
Ability to read and interpret documents such material masters, material specifications, material drawings, vendor certificates, etc. Identify assembly versus components of an assembly.
Demonstrate knowledge of various MRP types and impact to inventory level.
Ability to write routine correspondence with vendors.
Ability to accurately describe technical or material master discrepancies observed between the company’s requirements and vendor supplied materials.
Ability to speak effectively with customers, vendors, and internal partners.
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals
Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions.
Ability to deal with problems involving a few concrete variables in standardized situations.
Performs other related duties as assigned.

Education and experience:

Associates degree preferred or one to two years related experience and/or training; or equivalent combination of education and experience.
Minimum 2 years’ experience in buying/planning aspects of an integrated ERP environment, preferably with SAP.
Minimum 2 years’ experience in Purchasing and Vendor Management.
Supply Chain or Material Management experience, with spare parts knowledge a plus.
Professional certifications (CPIM, CSCP, ISM, APICS) preferred.

BEOCS

Date Added: 08-05-2022

Forklift Driver II - 3rd Shift

19642

Sturgis, Michigan

Manufacturing

Warehouse Worker - 2nd Shift

19640

Mansfield, Massachusetts

Manufacturing

Operator I

19638

Pleasanton, California

Manufacturing

BEPC has an open position for a Medical Device Assembler in Pleasanton CA!
Contract W2 Period: 6 month contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Full-time (shift: 5am-1:30pm)

DETAILS

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.

Education:
High school degree or equivalent preferred.

BEOCS

Date Added: 08-05-2022

Manufacturing Assembler / Operator 1 - Jaffrey

19636

Jaffrey, New Hampshire

Manufacturing

BEPC has an open position for a Manufacturing Assembler / Operator 1

Work location: Jaffrey, NH

Contract W2 Length 6-month contract with possibilities for extension.

Benefits: Medical, Vision, Dental, Life Insurance.

Shift: Monday - Friday 6:50am 2:50 pm

40 hours a week

Description

Performs a variety of equipment operating and adjusting duties such as assembling, mixing, cleaning, welding, bonding, inspecting, testing, labeling, packaging, etc. to fabricate and process products to meet high quality specifications following prescribed procedures.
Working from verbal and written instructions may use a variety of equipment including welders, hot air guns, scales, bonders, fillers, simple test equipment and other related supplies.
May use measuring instruments to ensure conformance to specified tolerances disassembles precision assemblies and corrects malfunctions. Makes accept/reject decisions, taking corrective action where possible.

Responsibilities

Capable of efficiently operating multiple operations according to SOP and within specifications.
Record all production data accurately, neatly and in accordance cGMP.
Continually assesses the quality of product being manufactured and act as a role model for new employees about product quality.
Notify Supervisor or Lead person if quality is in question and suggest appropriate course of action.
Make the most efficient use of work time by arriving to work on time, limiting break time to allotted time intervals and not distracting other operators during the workday.
Make improvements in personal efficiency to maximize what is accomplished each day and be able to meet difficult production goals in a consistent manner.
Works well with other operators and a team player.
Maintain a safe work environment by keeping work area neat and organized.
Understands all critical business metrics such as execution to master plan, scrap reduction and material accuracy, etc.
Make recommendations to supervisor to improve department regarding production metrics and overall manufacturing activities.
Anticipates, recognizes and controls safety hazards and environmental impacts associated with job function (e.g. identifies risk reduction and waste elimination opportunities, reports all incidents and near misses, completes all EHS related training, wears proper Personal Protective Equipment).

BEOCS

Date Added: 08-05-2022

Maintenance Technician I

19628

Westbrook, Maine

Other Area(s)

US - Principal Hardware Engineer

19627

Clearwater, Florida

Engineering

Scientist I - Pharmacokinetics

19626

South San Francisco, California

Biotech/R&D/Science

BEPC Inc. has a great job opportunity for a Scientist I in South San Francisco, CA!

W2 Contract for 6 months with opportunity for extensions.
Weekly pay and benefits: Medical, Dental, Vision and Life Insurance.

Job description:

The Preclinical and Translational PKPD (PTPK) Department is looking for an exceptional laboratory-based contract scientist to work in the investigative PK/ADME group in South San Francisco. This position is to investigate the pharmacokinetics, biodistribution, metabolism, and the PKPD relationships of novel therapeutics in preclinical setting in support of early and late-stage drug development.

The candidate will be responsible for designing and implementing in-vitro and in-vivo studies that includes cell based in-vitro assay, radiolabeled tissue distribution studies, ADME studies to understand the properties of protein and nucleotide therapeutics. The candidate will interact and develop close partnerships across various functions including Research, Safety Assessment, PD Biomarker, Bioanalytical Assays, Clinical Sciences, Formulation and Regulatory. Additional component of the job will be sample/data analysis and presentation of results to cross-functional teams, department meetings, review committees, internal/external conferences, and regulatory agencies.

Responsibilities:

Design and implement in-vitro and in-vivo studies to address ADME questions of protein and nucleotide therapeutic. Writing and submitting protocol to cross functional team for review.
Carry out sample analysis (including tissue processing) by using different analytical methods.
Characterize and identify possible biotransformation products from protein and nucleotide therapeutic in different biological matrices.
Interpret data and communicate results in department meeting and project team meeting.
Prepare presentation and report for conferences, manuscripts, and regulatory documents.

Desired profile and skills:

Highly motivated individual with a passion for science, a curiosity of solving complex problems, attention to detail, and a demonstrated effectiveness to work independently and in a team setting.
Proficiency in a broad variety of lab related technical skills (cell culturing, cell base assay, analytical chemistry, etc.).
Strong knowledge in basic pharmacology, drug metabolism (characterizing and identifying metabolite) and in PKPD relationship.
Strong communication and collaboration skills, along with the ability to clearly articulate solutions.

Requirements:

A Ph.D. in Pharmaceutical Sciences, Drug Metabolism, Pharmacology, Biochemistry or related discipline. 0-2 year of industry and/or post-doctoral experience is preferred.
Bachelor’s or Master’s degree in Biology or Biochemistry with 5-10 years in the Research and Development experience may also qualify.
Must have demonstrated a general working knowledge of cell-based assay, analytical techniques (HPLC, LSC, mass spectrometry etc.), and laboratory skills.
Understanding of PK concepts and the use of novel drug delivery system is preferred.
Previous experience working with analysis of nucleotide (mRNA, DNA, ASO, etc.) is preferred.
Previous experience in chemistry, especially with working with radioisotope, is a plus.
Good oral and written communication skills are important as well as demonstrated effectiveness in working independently and in a team setting.

BEOCS

Date Added: 08-04-2022

Sr Electrical Technician

19625

Glendale, Arizona

Technical

Sr Systems Engineer

19624

Glendale, Arizona

Engineering

Sr Advanced Software Engineer

19623

Clearwater, Florida

Engineering

BEPC is seeking a skilled Sr Advanced Software Engineer to join our fast-growing team of consultants in Clearwater, FL!

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

**Candidate must be local to Clearwater, FL to support onsite lab integration and test**

This role involves low level SW development of board support packages, including RTOS integration, device driver development and debugging of HW and SW in the development on aerospace electronic systems. Requires working knowledge of Ultrascale+, JIRA and Bitbucket. Experience with Lauterbach (or similar) debugging tool a plus. Possesses the ability to write test scripts to test SW features and to run regression tests. Knowledgeable in building the SW release. Also, coordinates work teams. Provides technical support to project team members.

Requirements:

Bachelor's degree in area of specialty
At least 8+ years of experience in the field or in a related area.
Demonstrates expertise in 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 provide consultation on complex projects and is considered a top-level contributor / specialist.
A wide degree of creativity and latitude is expected.
May report to an executive or a manager.

The subcontractor must have the following experience:

Software Development Life Cycle process development; requirements, design, implementation, unit and integration testing phases.
Embedded software development on ARM-based microcontrollers, ARMv7 and ARMv8 instruction sets
Developing device drivers for communication interface buses, such as PCIe, Serial I/O, IEEE-488
Utilizing Eclipse-based, cross compilation software development environments to build and debug software on target hardware
Utilizing and developing embedded software for Real-Time Operating Systems (RTOS)
Developing software using Quantum Leaps QP/C active object framework
Maintaining software under version control using SubVersion or similar Software version control systems
Utilizing Atlassian Jira (or similar) for issue tracking
Familiar with static code analysis tools
Familiar with Xilinx software development tools

BEPRO

Date Added: 08-04-2022

Sr Electronic Design Engineer

19621

Glendale, Arizona

Engineering

Principal Semiconductor Engineer

19620

Clearwater, Florida

Engineering

Manufacturing Operator 1

19614

Tempe, Arizona

Manufacturing

BEPC has an open position for a Manufacturing Operator in Tempe, AZ!
Contract W2 Period: 6-month contract with possibilities for extensions
Pay & Benefits: $24.00/hr. +Medical, Dental, Vision and Life Insurance
5am – 5pm

This site requires a mask while onsite
Forklift experience, certification a plus
Chemical handling and semiconductor experience a plus
Position will require to be on feet 80% of the time, able to climb ladders, bend and lift.

Duties:

Performs production procedures in accordance with Standard Operating Procedures (SOP), resulting in quality product. Formulation Tasks
Gather chemicals from different storage locations Blending 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
Maintaining safe working conditions and practices to achieve safety objectives
Maintain required safety documentation
Attending all mandatory site-specific training and meetings
Performing work duties in accordance with Quality Systems Manual procedures, safety policies and site-specific requirements.
Performing manufacturing, packaging and testing of products and various manufacturing systems throughout the facility
Consistently demonstrating skills to operate all equipment used in the department in a safe manner
Understanding each manufacturing process and being able to identify and report any deviations to the lead/manager in a timely manner
Utilizing automated programs and computer systems to help drive consistent and reliable manufacturing, packaging and testing
Inspecting all work areas on a continuous basis for any mechanical problems, safety hazards and unusual operating conditions
Keeping work and supply areas in a safe, clean and orderly condition at all times
Coordinating activities in production with other facility groups to ensure minimal impact to the production continuity
Collecting in process and finished product samples
Performing basic troubleshooting on equipment and making minor repairs or adjustments, as necessary
Submitting work orders to the maintenance planning system
Assisting with training and development of new employees
Assisting in generating and revising SOPs, as necessary
Contributing to continuous improvement in safety, quality and manufacturing efficiencies
Monitoring and replenishing in-process inventories of consumables/raw materials
Assisting in shipping/receiving activities as directed
Other duties as assigned

Requirements

High School Diploma/GED

Date Added: 08-04-2022

Operator II

19613

Scarborough, Maine

Manufacturing

BEPC has a Scarborough, ME area open position for an Operator to join our fast-growing team of consultants!

Contract W2 Period: 3 months with opportunity for extensions
+ Medical, Dental, Vision & Life Insurance

Work Shift: Flight D

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

High School Diploma or Equivalent

KEY QUALIFICATIONS:

This position is Nonexempt.
Hours over 40 will be paid at Time and a Half.
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

BEPRO

Date Added: 08-04-2022

Operator II

19612

Scarborough, Maine

Manufacturing

BEPC Inc is looking for an Operator II in Scarborough ME!
Contract W2 Period: 4 months contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

*2^nd Shift: (Sat – Tue / Sun – Tue) alternating weeks from 4:45pm – 5:15 am**

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: 08-04-2022

Operator II

19611

Scarborough, Maine

Manufacturing

BEPC Inc. has a great job opportunity for an Operator II in Scarborough, ME!

W2 Contract for 4 months with opportunity for extensions.
Weekly pay rate: $22.66 – $26.19 per hour.
Benefits: Medical, Dental, Vision and Life Insurance.

Job description:

This position is responsible for the production of high-quality medical devices on a team within a manufacturing cell, in the cleanroom environment. 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.

Essential Duties:

Assembles medical devices and related components.
Cleans tools and equipment per documented procedures.
Disposes hazardous waste material on corresponding hazardous waste areas.
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.

Flight A Shift:

From 4:45 a.m. to 5:15 p.m., on a rotating week schedule:

Week 1: Monday, Tuesday, Friday, Saturday, and Sunday.
Week 2: Wednesday and Thursday.

Desired skills:

Ability to be cross-trained.
Attention to detail.
Good manual dexterity.
Strong communication.
Dependability.
Cleanroom and catheter build experience is preferred.
Some machine operating experience.
Some computer experience.
Lifting and carrying boxes may be required.

Requirements:

High School Diploma or equivalent (GED).
2+ years of experience. Manufacturing experience will be preferred.

BEOCS

Date Added: 08-04-2022

Sr Advanced Systems Engineer

19610

Clearwater, Florida

Engineering

BEPC is seeking a skilled Sr Advanced Systems Engineer to join our fast-growing team of consultants in Clearwater, FL!

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

***Must be On-Site***

Minimum Qualifications:

BS in Electrical Engineering; MSEE preferred
4-6 years directly related professional experience performing radiation analysis.
Experience with most of the following: TID, ELDRS, DD, SEE, SEU, SEL, SEB/SEGR, SET, RLAT

Preferred Qualifications:

Experience in planning and execution of RLAT, SEE, and FXR tests on components and subsystems
Experience in using one or more radiation transport analysis (eg. GEANT4, MCNPX, NOVICE)
Experience in using one of more radiation rate calculation software (eg. SpaceRadiation, Crème 96, Spenvis)
Knowledge/experience in the effects of radiation on materials and components
Experience in analysis, control and mitigation for spacecraft charging
Understanding of NWE and how to interpret/mitigate, i.e. PD upset/transient/latch up/burnout, SGEMP, IEMP and fission byproducts.
RF domain knowledge
Experience in design and/or analysis of digital and analog circuits
Knowledge/experience in the effects of radiation on materials and components

Responsibilities:

Determine and specify space environments for systems, subsystems and components.
Understand space environment interactions with spacecraft components and materials.
Understand the man made/weapon environment and associated interactions with guidance and computer products.
Perform analysis and modeling of designs against expected environments to verify robustness.
Assist with requirements analysis and parts selection recommendations (eg. SCDs, PARs).
Apply understanding of Total Ionizing Dose, Displacement Damage, and Single Event Effects
Plan and execute component testing for TID, SEE, DD, Prompt Dose (Flash X-ray).
Prepare test reports, present results and achieve customer approvals.

BEPRO

Date Added: 08-04-2022

Operator I

19609

Scarborough, Maine

Manufacturing

BEPC Inc. is urgently looking for a Medical Device Operator I in Scarborough, ME.

W2 CONTRACT: 4 – month contract with opportunities for extensions.

PAY AND BENEFITS: $28.00/ hr. + Medical, Dental, Vision and Life Insurance.

Flight D: 12 hr. shifts.

Job description:

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 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.

Experience:

High school degree or equivalent preferred.

BEOCS

Date Added: 08-04-2022

Sr Advanced Systems Engineer

19607

Glendale, Arizona

Engineering

BEPC is seeking a skilled and experienced Sr Advanced Systems Engineer to join our fast-growing team of consultants in Glendale, AZ!

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

***On-site Position***

Minimum Qualifications:

BS in Electrical Engineering; MSEE preferred
4-6 years directly related professional experience performing radiation analysis.
Experience with most of the following: TID, ELDRS, DD, SEE, SEU, SEL, SEB/SEGR, SET, RLAT

Preferred Qualifications:

Experience in planning and execution of RLAT, SEE, and FXR tests on components and subsystems
Experience in using one or more radiation transport analysis (eg. GEANT4, MCNPX, NOVICE)
Experience in using one of more radiation rate calculation software (eg. SpaceRadiation, Crème 96, Spenvis)
Knowledge/experience in the effects of radiation on materials and components
Experience in analysis, control and mitigation for spacecraft charging
Understanding of NWE and how to interpret/mitigate, i.e. PD upset/transient/latch up/burnout, SGEMP, IEMP and fission byproducts.
RF domain knowledge
Experience in design and/or analysis of digital and analog circuits
Knowledge/experience in the effects of radiation on materials and components

Description:
Responsible for supporting the development of precision navigation and timing products and ensuring survivability in the on-orbit environment. This includes all phases of product development from initial architecture and development of interfaces and component requirements thru design, testing and verification, on to production support. Some products may require operational support and on-orbit anomaly resolution. Tasks will include characterization of space environment impacts on system performance, testing and selecting parts, and evaluation of alternative designs for optimum robustness and performance.

Responsibilities:

Determine and specify space environments for systems, subsystems and components.
Understand space environment interactions with spacecraft components and materials.
Understand the man made/weapon environment and associated interactions with guidance and computer products.
Perform analysis and modeling of designs against expected environments to verify robustness.
Assist with requirements analysis and parts selection recommendations (eg. SCDs, PARs).
Apply understanding of Total Ionizing Dose, Displacement Damage, and Single Event Effects
Plan and execute component testing for TID, SEE, DD, Prompt Dose (Flash X-ray).
Prepare test reports, present results and achieve customer approvals.

Bepro

Date Added: 08-04-2022

Operator I

19606

Scarborough, Maine

Manufacturing

BEPC Inc. is urgently looking for a Medical Device Operator I in Scarborough, ME.

W2 CONTRACT: 4 – month contract with opportunities for extensions.

PAY AND BENEFITS: $28.00/ hr. + Medical, Dental, Vision and Life Insurance.

Flight B: 12 hr. shifts.

Job description:

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 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.

Experience:

High school degree or equivalent preferred.

BEOCS

Date Added: 08-04-2022

Operator I

19605

Scarborough, Maine

Manufacturing

BEPC Inc is looking for an Operator I in Scarborough ME!
Contract W2 Period: 4 months contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

*1^st Shift: (Mon, Tue, Fri, Sat, Sun / Wed, Tue, Mon, Tue) alternating weeks from 4:45am – 5:15 pm**

Description:

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: 08-04-2022

Scientist I - Oncology Biomarker Development

19604

South San Francisco, California

Biotech/R&D/Science

BEPC Inc. has a great job opportunity for a Scientist I in South San Francisco, CA!

W2 Contract for 11 months with opportunity for extensions.
Weekly pay and benefits: Medical, Dental, Vision and Life Insurance.

Job description:

The Department of Oncology Biomarker Development (OBD) is seeking a highly motivated Scientist to contribute to the discovery and development of biomarkers in support of the company’s extensive cancer immunotherapy (CIT) portfolio.

The successful candidate should have demonstrated experience in use and application of current theories, principles, and cutting-edge techniques relevant to immunology, cancer biology, biomarker science, data analysis, and assay development. The applicant should be knowledgeable in drug development as it relates to his/her technical expertise and is able to apply this knowledge to projects. Demonstrates consistent effective communication of ideas, goals, and results. Consistently demonstrates ability to independently design and carry out experiments and/or data analyses that address significant drug development questions.

Responsibilities:

Responsible for translational research to enable the development of biomarkers and assays for use in the clinical development of novel drug candidates.
Experimental strategies will include the application of state of the art molecular and genomic technologies to analyze clinical samples.
Specific responsibilities will include processing and analyzing clinical trial samples, data analysis and presentation, and contributing to experimental design and planning.
Demonstrates independence in the design of subsequent experiments upon interpretation of data.
Develops, tests, and refines new methods and/or data analyses to address project needs.
Broadly recognized as a technical expert in the application of cutting-edge biomarker science.
Presents work at internal and external meetings, conferences, and workshops (as applicable). Presentations are clear and effective.

Education and experience required:

Master’s degree with +6 years or Ph.D. with +2 years of relevant work/educational experience and hands-on laboratory research experience.
Must have an intimate knowledge of, and extensive hands-on experience with, relevant molecular and cell biology, and immunology techniques (e.g., tissue processing, high dimensional flow cytometry, single cell RNASeq, primary and derivative cell isolation and culture, ELISA based immunoassays, etc.).
Preferred candidates will have interest and experience in genomic data (RNASeq, WES) analysis tools.
Preferred candidates will have experience in oncology, development of biomarker assays, and their implementation in clinical trials.
Candidates must have excellent communication skills and the ability to work with scientists and associates from multiple laboratories, disciplines, and departments.
A proven track record, including authorship of and/or contributions to, publications in top tier journals is desirable.

BEOCS

Date Added: 08-03-2022

Electrical CAD Technician.

19603

Columbus, Ohio

Professional

Batchmaker - Crew 6

19601

Fairfield, California

Manufacturing

Audit Clerk

19600

Cincinnati, Ohio

Technical

Forklift Driver II

19593

Columbus, Ohio

Manufacturing

Analytical Technician II

19592

San Jose, California

Logistics/Transportation

Operator II

19586

Temecula, California

Manufacturing

BEPC is actively looking for Medical Device Assembly in the Temecula, CA area!!
1 year contract with possible extensions!!

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. P
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.

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 experience

BEOCS

Date Added: 08-02-2022

Sr Product Design Engineer

19585

Plymouth, Minnesota

Engineering

Project Coordinator

19584

Remote, Texas

Professional

BEPC has an open position for a Project Controller/Coordinator!

Location: Remote
Contract Length: 1 year contract with possibilities for extensions
Benefits: Medical, Dental, Vision and Life Insurance

Core Purpose of the role:

To work with the Program Director, workstream leaders, and project leaders to implement agreed project planning, monitoring, and control processes to ensure the tracking and reporting is accurate and timely across the program.

Specific key accountabilities:

The project controller/scheduler is responsible for:

Implementing the agreed project planning, scheduling, management, and controlling processes
Supporting the workstream and project managers to produce project and resource plans in line with agreed processes.
Reviewing and approving all project plans to ensure adherence to agreed formats and approach
Providing challenge to the project leaders on content and approach of project plans
Working with the workstream leaders and project leaders to identify, resolve, and report on issues, risks, and challenges
Reviewing, monitoring, and reporting on the progress and trends of projects against the agreed metrics up through to the PMO
Identifying potential risks and issues at project and resource level and report to workstream leaders and the Program Manager
Administering the RADIO and other program management processes
Creating detailed project with the project leaders and ensuring that the activities integrate at a project and workstream level
Integrating the projects at a level agreed, creating mid-level plans, milestone plans and baseline the Master Schedule.

Short Term Objectives:

Communicate planning processes to project leaders
Work with project leaders to create detailed project plans
Create the program structure and management tools
Create the monitoring and reporting processes
Implement the agreed PMO processes and procedures

Key success measures:

Consistent project planning and management approach
An integrated master schedule in place and baselined
Project controls and review processes operating effectively
Timely and accurate reporting against the agreed metrics
RADIO process operating effectively

BEOCS

Date Added: 08-02-2022

Description: Inspects, labels and packages raw and finished products. May be required to maintain records according to Good Manufacturing Practices. May be working in a clean-room environment. Moderate supervision is required. Tier Level 2 BEOCS