Subject: Construction Safety Support
Job Overview:
EHS issues associated with facility and process equipment construction range from managing permits appropriately to assessing building materials to accurately understand the hazards. Appropriate identification and definition of these issues can reduce the potential for cost growth during the construction process and/or risks of potential non-compliance and subsequent government issued fines.
A number of factors can contribute to increases in safety incidents during facility constructions including employee turnover and changing site conditions. A strong safety presence onsite during this transition period is key to minimizing safety incidents. Johnson & Johnsons has found that this is most effectively addressed through regular safety observations and coaching to identify and mitigate potential hazards.
Experience should include facility construction experience and capital project support for the ETO Abatement Project in San Angelo, TX. Support is anticipated throughout the life cycle of a project. We are seeking proposals from companies that have a proven record of promoting effective planning, safe work execution, driving regulatory compliance, and preventing project cost and schedule creep.
The role of the construction safety DRI will be, but not limited to, as follows:
SCOPE OF WORK
Support the ETO Abatement Project San Angelo, TX site. The project is expected to begin in June 2020 and terminate in July 2021. We anticipate the scope of work will be conducted primarily by an experienced construction safety consultant. We will assist in the day-to-day application of EHS/CSS program including inspections, safety and compliance walks, root-cause analysis, and contractor review. Construction work will be scheduled for day shift.
Proposed 40 hours per week will be primarily focused to construction safety. Onsite work is expected to be 5 days per week on average.
BEOCS
BEPC is actively looking for a Drug Manufacturing Technician in the Gretna, LA area!
5 month contract with possible extensions!
Benefits include Medical, Dental, Vision, and Life Insurance
Pay Rate: $12.00-$15.00
Shift: Tuesday-Saturday 10:30am-3:30pm
Job Duties:
BEPC has an open position for a Research Associate III in South San Francisco, CA!!
Contract W2 Period: 12month contract with possibilities for extensions.
Pay & Benefits: $43-$50/hr. + Medical, Dental, Vision and Life Insurance
The mission of the Investigative Toxicology group is to elucidate the mechanisms underlying toxicities that are observed non-clinically and/or in clinical trials through hypothesis driven research.
This process involves closely collaborating with scientists across the organization to support the overall safety assessment for our novel therapeutics spanning drug discovery through clinical development and marketing.
The group provides fit-for-purpose wet lab-based investigation to address target safety assessment, lead optimization, and issue mitigation by employing state-of-the-science in vitro and ex vivo approaches.
As such, we are constantly establishing new platforms and technologies to support a constantly changing portfolio, novel modalities, and emerging therapeutic area needs.
We are looking for a highly motivated candidate to work in collaboration with other researchers in the Investigative Toxicology lab.
This individual must have experience in cell culture and will be responsible for: culturing and expanding primary cells and cell lines for in vitro screenings, treating and performing assays to assess cytotoxicity and metabolic changes of cells, capturing cell culture images using confocal and high content imaging.
This individual will be working with cells from a broad range of tissues (liver, GI, vascular, ocular) and is expected to make detailed observations related to experiments, perform, analyze data, and interpret results. He/she will contribute with scientific insights and also work in projects related to peer review publications.
The individual will also participate in projects related to the development of microfluidics platforms to support toxicity testing for our drug discovery program.
Job Description
The Investigative Toxicology group's goal is to use ex vivo and in vitro tools to assess safety liabilities and mechanisms of toxicity observed pre-clinically to support the entire portfolio spanning discovery through development.
This laboratory-based role involves performing, qualifying and implementing biological assays and technologies to support the Investigative Toxicology group.
They will also contribute to ongoing efforts to understand the impact of complex-in-vitro models in hazard id and liability assessment.
This is an ideal position for a researcher who is enthusiastic about learning and contributing to projects with a broad range of techniques.
As such the position requires excellent communication and collaboration skills, a desire to learn about and integrate multiple aspects of drug toxicity, and a passion for lab-based research. In particular a candidate who will be successful in this role will be able to collaborate with subject matter experts to collaboratively design a scope of work and key performance indicators for a research project, but then independently drive forward the experimental work including towards identified milestones.
Additionally, the success in this role will require flexibility and a willingness to learn new model systems as well as initiative to troubleshoot unexpected experimental results or limitations.
Skills:
- Candidate will provide scientific and technical support to assays and platforms supported or under development by the Investigative Toxicology group by:
- Performing experiments involving immortalized and primary cell culture, cell viability assessment, ELISAs, gene expression analysis, high content screening, confocal microscopy, and flow cytometry. Experience with these methodologies is desirable, but not required.
- A large portion of the cell culture work conducted will focus on the use of organoid or other complex in-vitro model (CIVM) systems
- Maintaining documentation related to protocol execution and results.
- Writing protocols and contributing to final reports as appropriate.
- Adhering to departmental SOPs to ensure study integrity and quality.
- Conducting experiments with a high level of independence and initiative.
- Performing tasks with minimal direct supervision for routine methods and studies commonly employed by the team.
Education:
- Bachelors (BS/BA) in pharmacology, pharmaceutical science, biology, bioengineering, chemistry, physiology, or related discipline is required; Masters (MS) degree is desirable, but not required.
Technical Experience Requirements:
- 1-3+ years of laboratory experience with hypothesis-driven research.
- Ability to analyze, integrate, and present data in a presentation is required.
- Experience with immortalized and/or primary cell culture, cell viability assessment, ELISAs, gene expression analysis, high content screening, confocal microscopy, and flow cytometry is highly desired.
- Experience with complex in-vitro model systems is highly desired.
Second Job Title:
- Scientific Researcher, Investigative Toxicology
Role will Involve:
- Sitting or standing for extended periods.
- Performing repetitive tasks such as cell culture, pipetting and labeling tubes.
- Collaboration across the Investigative Toxicology team and with key stakeholders.
- Work with potentially hazardous materials including (but not limited to): chemotherapeutics, biological hazards, and human primary cells.
BEOCS
BEPC Inc. is searching for a Warehouse Associate in Portsmouth, VA.
CONTRACT W2: 6 – month contract with possibilities for extensions.
PAY AND BENEFITS: $12.00 – 16.00/hr. + medical, dental, vision and life insurance.
8 a.m. – 4:30 p.m.
Responsibilities:
BEPC is actively looking for a Warehouse Operator 2 in St. Louis, MO!
12-month contract with possible extension!
Benefits include medical, dental, vision, and life!
Pay Rate: $18.00 - $21.00
Schedule: Monday - Friday 7:00 AM - 3:30 PM (1st Shift)
Summary of Duties and Responsibilities:
When receiving:
BEPC is actively seeking an Operator for 1st shift in the Plano, TX area!
W2 contract: 12 months w/ possible extensions
Pay rate: $16 - $18.41/hr
Benefits: Medical, Dental, Vision & Life Insurance
Shift: 6:00am - 4:30pm M - THUR
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.
MINIMUM JOB REQUIREMENTS:
BEPC Inc. is looking for an Engineering Technician in Clearwater, FL
PAID WEEKLY!!!
Work Location: On-Site
Contract: W2 Length (-month contract with possibilities for extensions)
Benefits: Medical, Vision, Health Care, 25K Life Insurance
Education: Associates Degree, Technical School Diploma, or two year’s college coursework in Electronics or related discipline.
Work Experience: 2 or more years electronics systems test experience or related field.
Shift: 1st Shift
Pay rate: $20.00 - $25.00
Job specific Competencies & Skills
Coordinates standard calibration processes on a variety of aerospace navigation equipment and records and analyzes results. Requires knowledge of industry specific tests and testing equipment. Requires 2-4 years of experience in the field or in a related area. Familiar with standard concepts, practices, and procedures within a particular field. Relies on limited experience and judgment to plan and accomplish goals. Performs a variety of tasks. Works under direct supervision. A certain degree of creativity and latitude is required. Typically reports to a supervisor.
This Lead Engineering Technician position is within the Space Inertial Navigation Test group. The Technician will be responsible for performing hands-on diverse technical tasks related to the calibration of Inertial Guidance and Navigation test equipment. Technician will be capable of providing work direction and technical training and guidance to other technicians as needed.
Work with technicians and engineers to resolve calibration and test setup and execution issues. Job requires physical exertion and extended standing, walking, sitting times while retaining focus on tasks at hand. Must keep detailed logs, follow detailed calibration procedures without error and provide daily status to program personnel (both verbal and written documentation). Execute 5S, Safety, equipment/lab maintenance and other tasks on a daily basis; demonstrate commitment to continuous improvement.
Basic Qualifications:
• Associates Degree, Technical School Diploma, or two year’s college coursework in Electronics or related discipline.
• Two or more years electronics systems test experience or related field.
BEPRO
BEPC has an open position for Pathology Research & Early Development - Algorithm Engineer / Data Scientist in Tucson, AZ!!
Contract W2 Period: 18-month contract with possibilities for extensions.
Pay & Benefits: $46-$54/hr. + Medical, Dental, Vision and Life Insurance
Hybrid worker - 2-3 days onsite in Tucson
Works with a highly collaborative team of imaging scientists and software developers to solve image and data analysis problems in the field of Digital Pathology.
Contributes to algorithm development activities for technology assessment, internal project collaborations, and commercial medical devices. Implements technology in the fields of image processing, machine learning, pattern recognition and data mining.
Organizes and tracks own deliverables.
Responsibilities
Implements or modifies existing algorithms to analyze histopathology images and data.
Leads algorithm development/experiments to analyze histopathology images.
Implements software in prototyping and commercial product development environments.
Collaborates with other members of a project team to meet defined scientific and technical goals/requirements.
Interacts in a multidisciplinary environment with internal and external stakeholders (e.g., pathologists, biochemists, instrumentation engineers, software engineers, and marketing representatives).
Keeps up to date with technology advances and job training requirements in the medical device industry.
Identifies and documents Intellectual Property opportunities for technology and applications.
Presents results to project partners, collaboration partners within the Roche group, customers, and at scientific conferences.
Other duties as assigned by management.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each responsibility satisfactorily.
The requirements listed below are representative of the knowledge, skills, and/or abilities required.
Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities.
Formal Training/Education Details Req Pref Master's Degree Computer Science, Biomedical Engineering, Electrical Engineering, or a related field. Ph.D. Computer Science, Biomedical Engineering, Electrical Engineering, or a related field.
Experience in the design and development of analysis algorithms for biomedical image data.
Hands-on experience with algorithm development for image or data analysis algorithms.
Extensive experience with commonly used Deep Learning models and frameworks (e.g., Pytorch, Fastai, TensorFlow).
Product development experience with a focus on data analysis.
Experience working with Digital Pathology tools or Software.
Experience working with medical devices.
Are equivalencies acceptable? No Knowledge, Skills and Abilities Knowledge, Skill or Ability Req Pref Proficiency
Excellent written and verbal communication skills.
Excellent skill sets in Matlab, C++ or Python.
Good understanding of scientific principles; good analytical and mathematical skills.
Working knowledge and theoretical understanding of image analysis, pattern recognition, machine learning, computer vision, and data mining methods.
Understanding and following of software engineering practices for prototyping and commercial product development languages.
Basic understanding of biomedical image data, preferably in digital pathology.
BEOCS
BEPC is actively looking for an Associate Dia Tech Packaging in Branchburg, NJ area!
6-month contract with possible extensions!
Benefits include medical, dental, vision, and life insurance
Pay Rate: $16.80 $19.80/hr.
2 Shift – Onsite role.
Job requirements will include ability to perform in the aseptic environment. Wear personal protective equipment, such as eye, foot, lab coat, mask, gowning coveralls.
Summary of Duties and Responsibilities:
• Assembles totes, cartons, platforms, and associated packaging and filling components. Under direction of area supervision, assist in setting up Packaging/Filling lines, and staging for production activities.
• Perform visual inspection for visible defects of components produced in the Filling Area and components being placed into kits in the Packaging Area.
• Place components (filled vials, inserts, barcode clips etc.) into totes and or kits per instructions in applicable SOPs and Production Records.
• At conclusion of Fill/Pack operation, count and reconcile intermediates, labels, inserts etc.
• Palletize finish product and assist in moving production materials from Fill/Pack lines to refrigerated and general warehouse areas.
• Understands GMP, QSR, ISO and RMS quality regulations.
Qualifications:
• High School Diploma/GED
• Seeking candidates 1+ years’ experience.
• Attention to detail.
• Ability to organize and prioritize multiple tasks and responsibilities.
• Candidates' attitude, professionalism, eagerness, ability to learn quickly and adaptiveness is essential to success.
• Prior experience working in a clean room, production and or packaging operations is desirable but not required.
BEOCS
BEPC is looking for an Associate Dia Tech- Liat D1 in Branchburg, NJ to join our fast-growing team of consultants!
W2 Contract: 6 months with opportunities for extensions based on business needs and performance.
Pay Range: $18.90-21.00/hr. plus we offer Medical, Dental, Vision and Life Insurance benefits!
Schedule: 100% Onsite, Mon-Wed, 6 a.m. - 7 p.m.
Job Summary:
Job requirements will include ability to perform in the aseptic environment. Wear personal protective equipment, such as eye, foot, lab coat, mask, gowning coveralls.
Responsibilities:
BEPC has an open position for an Assoc Dia Tech-Liat D1 in Branchburg, NJ!!
Contract W2 Period: 6-month contract with possibilities for extensions.
Pay & Benefits: $18-$20/hr. + Medical, Dental, Vision and Life Insurance
HS Diploma Required
0-2 years' experience in an "Operations/Production environment " or filling, labeling or warehouse operations or equivalent combination of education and experience.
Experience in medical device or related industry preferred.
Job requirements will include ability to perform in the aseptic environment. Wear personal protective equipment, such as eye, foot, lab coat, mask, gowning coveralls.
Responsibilities
• Assembles totes, cartons, platforms, and associated packaging and filling components. Under direction of area supervision, assist in setting up Packaging/Filling lines, and staging for production activities.
• Perform visual inspection for visible defects of components produced in the Filling Area and components being placed into kits in the Packaging Area.
• Place components (filled vials, inserts, barcode clips ect.) into totes and or kits per instructions in applicable SOPs and Production Records.
• At conclusion of Fill/Pack operation, count and reconcile intermediates, labels, inserts etc.
• Palletize finish product and assist in moving production materials from Fill/Pack lines to refrigerated and general warehouse areas.
• Understands GMP, QSR, ISO and RMS Quality regulations and ensures operations are performed according to those requirements.
BEOCS
BEPC is actively looking for a Production Tech in the Scottsdale, AZ area!!
Contract length is 8 months with possible extensions!
Benefits include medical, dental, vision and life!
Pay rate is $18.00-$20.90 per hour WEEKLY PAY!
Shift: Monday-Thursday from 2:30pm-1:00am (2nd shift)
Responsible for manufacturing products, supporting production issues, assisting with the installation and qualification of production equipment, assisting with equipment maintenance, building prototypes, and assisting in other areas as necessary. Takes direction from Manufacturing Supervisor or higher.
Requirements:
BEPC is actively seeking an Engineering Skilled Trade Project Manager in the Santa Clara, CA area!
W2 contract: 12 months w/ possible extensions
Pay rate: $52 - $56.58/hr
Benefits: Medical, Dental, Vision & Life Insurance
Shift: 7am - 3:30pm
EMD Electronics is seeking a Project Coordinator to work onsite at customer sites located in Santa Clara, CA. This is a challenging, hands-on, rewarding job opportunity for people who want to join a growing business
MINIMUM JOB REQUIREMENTS:
BEPC Inc. is looking for an Manufacturing Engineer in St. Louis, MO
PAID WEEKLY!!!
Work Location: On-Site
Contract: W2 Length (12-month contract with possibilities for extensions)
Benefits: Medical, Vision, Health Care, 25K Life Insurance
Education: High School Diploma, GED, or equivalent required. Associate or technical degree preferred.
Work Experience1-3 years of working in a similar environment preferred.
Shift: 6:00PM – 6:00AM
Pay rate: $19 - $22.50
Job specific Competencies & Skills
• Ability to operate powered industrial equipment, Reactor systems, Industrial centrifuges and dryers, Ion exchange columns, and DCS systems. SAP, Word, Excel, Access, experience a plus.
• Knowledge of product flow throughout the manufacturing process.
• Ability to effectively communicate in a professional manner with all levels of staff both orally and written.
• Ability to work in a group setting.
• Ability to demonstrate attention to detail.
• Ability to work quickly and adjust to changing priorities in a fast-paced environment.
• Demonstrated problem-solving and team building skills with the ability to work with a diverse group of people.
Essential Job Functions:
• Engages in problem solving and performance management within the business area the team leader is responsible for
• Assists Supervisor to maintain workflow in department
• Provides training for new personnel as needed
• Maintains high-quality work environment by sharing knowledge and experiences so team members are motivated to perform at their highest level
• Keeps supervisor informed of potential and/or existing concerns
• Leads by example in performing core manufacturing job elements by meeting or exceeding performance expectations, following health and safety guidelines, job accuracy, and following company and regulatory requirements.
• Participates in and supports the development and implementation of process improvement projects including test cycles to challenge current practices, improve system efficiency, enhance customer service, and maintain compliance
• Troubleshoot problems within the department – including root cause analysis and development of solutions to avoid future occurrences
• Demonstrates working knowledge of department operating systems.
• Maintains orders, work areas and stock locations in a safe, clean, and organized manner.
• Reports unsafe or potentially unsafe hazards to any member of management
• Miscellaneous duties and tasks as assigned
• Exemplary attendance and adherence to schedule
BEPRO
BEPC Inc. is looking for an Manufacturing Engineer in St. Louis, MO
PAID WEEKLY!!!
Work Location: On-Site
Contract: W2 Length (12-month contract with possibilities for extensions)
Benefits: Medical, Vision, Health Care, 25K Life Insurance
Education: High School Diploma, GED, or equivalent required. Associate or technical degree preferred.
Work Experience1-3 years of working in a similar environment preferred.
Shift: 6:00PM – 6:00AM
Pay rate: $19 - $22.50
Job specific Competencies & Skills
• Ability to operate powered industrial equipment, Reactor systems, Industrial centrifuges and dryers, Ion exchange columns, and DCS systems. SAP, Word, Excel, Access, experience a plus.
• Knowledge of product flow throughout the manufacturing process.
• Ability to effectively communicate in a professional manner with all levels of staff both orally and written.
• Ability to work in a group setting.
• Ability to demonstrate attention to detail.
• Ability to work quickly and adjust to changing priorities in a fast-paced environment.
• Demonstrated problem-solving and team building skills with the ability to work with a diverse group of people.
Essential Job Functions:
• Engages in problem solving and performance management within the business area the team leader is responsible for
• Assists Supervisor to maintain workflow in department
• Provides training for new personnel as needed
• Maintains high-quality work environment by sharing knowledge and experiences so team members are motivated to perform at their highest level
• Keeps supervisor informed of potential and/or existing concerns
• Leads by example in performing core manufacturing job elements by meeting or exceeding performance expectations, following health and safety guidelines, job accuracy, and following company and regulatory requirements.
• Participates in and supports the development and implementation of process improvement projects including test cycles to challenge current practices, improve system efficiency, enhance customer service, and maintain compliance
• Troubleshoot problems within the department – including root cause analysis and development of solutions to avoid future occurrences
• Demonstrates working knowledge of department operating systems.
• Maintains orders, work areas and stock locations in a safe, clean, and organized manner.
• Reports unsafe or potentially unsafe hazards to any member of management
• Miscellaneous duties and tasks as assigned
• Exemplary attendance and adherence to schedule
BEPRO
BEPC has an open position for Quality Assurance Document Translator in Rocklin, CA!
Contract W2 Period: 12-month contract with possibilities for extensions
Pay & Benefits: $28.00 - $30.00/hr. +Medical, Dental, Vision and Life Insurance
Requirements
High School Diploma/GED
Experience with translation industry.
Excellent communication skills
Description:
BEPC has an open position for Complaint Investigations Technician in Alameda, CA!
Contract W2 Period: 6-month contract with possibilities for extensions
Pay & Benefits: $25.00 $30.18/hr. +Medical, Dental, Vision and Life Insurance
5am-1:30PM
BEPC is looking for a Retention Marketing Specialist in Newark, NJ to join our fast-growing team of consultants!
W2 Contract: 8+ months with opportunities for extensions based on business needs and performance.
**Hybrid Position in Newark, NJ**
Pay Range: $34.38-60.14/hr. plus we offer Medical, Dental, Vision and Life Insurance benefits!
Job Summary:
As a growth marketer this role will drive retention initiatives to improve customer lifecycle experience. You will conceptualize, execute, and automate marketing campaigns through various stages of the customer journey and lead experimentation across the company’s apps and website.
Responsibilities include:
Campaign Strategy:
BEPC is actively looking for an Associate Dia Tech Filling/Packaging in Branchburg, NJ area!
6-month contract with possible extensions!
Benefits include medical, dental, vision, and life insurance
Pay Rate: $16.80 $19.80/hr.
2 Shift: 3pm-11:30pm Monday - Friday
Performs duties related to filling, packaging, and warehousing of products (kits) containing various components in accordance with industry standards and applicable regulatory requirements.
Job requirements will include ability to perform in the aseptic environment. Wear personal protective equipment, such as eye, foot, lab coat, mask, gowning coveralls.
Summary of Duties and Responsibilities:
• Assembles totes, cartons, platforms, and associated packaging and filling components. Under direction of area supervision, assist in setting up Packaging/Filling lines, and staging for production activities.
• Perform visual inspection for visible defects of components produced in the Filling Area and components being placed into kits in the Packaging Area.
• Place components (filled vials, inserts, barcode clips etc.) into totes and or kits per instructions in applicable SOPs and Production Records.
• At conclusion of Fill/Pack operation, count and reconcile intermediates, labels, inserts etc.
• Palletize finish product and assist in moving production materials from Fill/Pack lines to refrigerated and general warehouse areas.
• Assists and monitors filling, labeling and packaging/warehouse equipment of varying complexity in accordance with SOPs, production batch records and filling records and packaging records.
• Assists in completing all necessary documentation associated with filling and packaging operations as required. (Batch production records and associated MRP system transactions) to ensure all components meet requirements pertaining to lot numbers, expiration dates, reconciliation, etc.
• Understands GMP, QSR, ISO and RMS quality regulations.
Qualifications:
• High School Diploma/GED
• Seeking entry level candidates 0-1 years’ experience.
• Attention to detail.
• Ability to organize and prioritize multiple tasks and responsibilities.
• Candidates' attitude, professionalism, eagerness, ability to learn quickly and adaptiveness is essential to success.
• Prior experience working in a clean room, production and or packaging operations is desirable but not required.
• Lifting up to 50lbs.
BEOCS
BEPC is hiring a REMOTE Supplier Quality Compliance Engineer
JOB DESCRIPTION
Summary/Objective:
The Supplier Quality Compliance Engineer ensures the execution of quality system compliance activities associated with the receipt and acceptance of robust supplier audit responses for identified supplier audit observations. The Supplier Quality Compliance Engineer performs these activities to applicable quality management system standards for fortune 500 Medical Device Companies. The Supplier Quality Compliance Engineer addresses supplier audit responses for suppliers across different industries such as Medical device, Pharmaceutical, Biotechnology, Microbiology and Sterilization Sciences as needed to meet customer requirements.
This individual will be responsible for supporting external inspections of External Manufacturers and Suppliers. They will also be responsible for supporting internal audits of the client’s Compliance program. Supports in the management, tracking to closure of External Manufacturers and Suppliers commitments to mitigation of identified risks. Supports in the completion of Follow Up reports related to the tracking and completion of External Manufacturing commitments taken to mitigate identified risks.
Responsibilities:
Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and client procedures and guidelines, this position:
• Assists in the development, implementation and continuous improvement of the client’s Compliance program.
• Ensures timely mitigation of risks identified through Supplier Audit Program.
• Requests and reviews documentation related to Supplier Audit Response for identified audit observations
• Assures that related client Compliance Quality Records are updated in a timely manner and are compliant with company procedures and policies. • Ensures timely completion of activities related to training.
• Proactively engages with external partners to develop a robust supplier corrective action response.
• Issues Follow Up reports in accordance with client procedural requirements.
• Identify process improvements related to standard operating procedures and systems to mitigate risk and drive a quality culture.
• Complies with policies, procedures, training requirements and company and regulatory rules and norms.
• Performs according to the company's quality policy and corporate rules in all business activities with providers and customers within and outside the company
• Escalates abnormalities and business critical information to the client’s Compliance Leadership.
•Maintains quality records where applicable per client records retention procedures.
• Responsible for ensuring personal and client Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
• Primary duty includes the exercise of discretion and independent judgment with respect to matters of significance.
Other Duties:
Other duties may be assigned as required by BEPC management.
Competencies:
• Expertise on/detailed knowledge of regulatory requirements in the FDA/ISO/Health Authority regulated industry (medical devices or pharmaceutical), with the ability to relate them to business/quality issues.
• Excellent prioritization skills
• Excellent written and oral communication skills as well as report writing
• Strong collaboration and influence skills to partner effectively both internally and externally
• Experience in the Medical Device industry or medical field
• Able to enter data on spread sheet and database applications
• Ability to make the complex clear and easily understood by others
• Knowledge of ISO 13485 and 21CFR 820
• Quality system auditor qualifications desirable, e.g., ASQ CQA or CBA, ISO 9001/13485 lead auditor
• Ability to work in a sometimes stressful fast paced environment
Supervisory Responsibility:
This position is an individual contributor position.
Work Environment:
This job operates in a professional office environment. This role routinely uses standard office equipment such as laptop computers and smartphones.
Position Type/Expected Hours of Work:
This is a full-time position, and hours of work typically Monday through Friday, 8:00 a.m. to 5:00 p.m. local time. However, agility and quick response time to customer and employee requests may be required at other times to include evening and weekends. This position will work remotely.
Travel:
This position requires minimal to no travel, e.g., < 5% as required to meet customer & business needs.
Required Education and Experience:
• Bachelor’s degree or equivalent required; concentration in Engineering or technical field preferred
• 5-8 years or more experience in a FDA regulated industry (pharmaceutical or medical devices) or another highly regulated industry is required.
AAP/EEO Statement
BEPC Inc. policy is to affirmatively implement equal opportunity for all employees and applicants for employment without regard to race, color, religion, sex, national origin, disability, military status, genetic information, or any other basis prohibited by law. Additionally, BEPC Inc. does not discriminate against an employee or applicant who acts to oppose such discrimination or participates in the investigation of a complaint related to discriminatory employment practice. Employment decisions will be made on the basis of each applicant’s job qualifications, experience, and abilities.
BEOCS
BEPC is actively seeking a Production Worker for 3rd shift in the Altavista, VA area!
W2 contract: 3 months w/ possible extensions!
Pay rate: $13 - $14.30/hr
Shift: 10pm - 6:30am
MINIMUM JOB REQUIREMENTS:
BEPC, Inc is seeking a Lab Design Specialist in Indianapolis, IN!!
W2 contract: Approximately 12 months with the possibility of extensions based on business needs & performance.
Benefits: Medical, Dental, Vision & Life Insurance
Pay Rate: $40.00- $45.00
Shift: 8am- 5pm
Summary
The Laboratory Design Specialist prepares 2D/3D designs and construction plans for complex automated and standalone laboratory solutions.The Laboratory Design Specialist supports the development of the laboratory design throughout multiple phases to ensure the successful implementation of the proposed solution.The Lab Design Specialist creates intermediate 3D visualization and digital images to promote the sales opportunity and support marketing needs.This off-campus position is a part of the Business Operation team and works closely with colleagues, as well as internal and external stakeholders (global business affiliates, field engineers, architects, customers, and others) to address the customers’ unique design requirements. While this is a remote position, it may require up to 10% overnight travel across the US.
Responsibilities
BEPC is looking for an Associate Dia Tech: Filling-1st Shift in Branchburg, NJ to join our fast-growing team of consultants!
W2-Contract: 6 months with opportunities for extensions based on business needs and performance.
Pay Range: $16.00-18.00/hr. plus we offer Medical, Dental, Vision and Life Insurance benefits!
Schedule: 100% Onsite, 7 a.m. - 3:30 p.m.
Job Summary:
Performs duties related to filling, packaging, and warehousing of products (kits) containing various
components in accordance with industry standards and applicable regulatory requirements.
Responsibilities:
BEPC is actively looking for Packing Operator 1 in the Martin, SC area!
6-month contract with possible extension!
Benefits: medical, dental, vision, and life insurance.
Pay Rate: $18.00-$21.00/hr
Shift:
2 week rotating schedule:
BEPC is hiring a Quality Operations Technician - Contractor in Irving TX
W2 - 1 year contract
Benefits include medical, dental, vision and life
Pay rate is $17.00-$19.00 per hour
JOB SUMMARY
Responsible for conducting technical quality assurance inspections, quality issue resolution, product containment, and supporting quality improvements for production processes and standards.
DUTIES AND RESPONSABILITIES
• Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
• Supports Quality Operation functions including: CAPA/NC initiatives, Quality “presence” on the manufacturing floors, and proactive GDP and Data Integrity.
• Assist with data collection for quality metrics, quality improvement initiatives, CAPAs, NCs, or Quality Systems.
• Perform data searches and transactions within MES, JDE, and EtQ.
• Partner with QEs and business partners (and other NC “owners”) providing support with NC process, investigations, and/or corrective actions.
• Actively influence the team and other fellow workers as role model for Collaboration and Teamwork.
• Primary coordinator for APMER related items such as request, documentation, closure, and transactions.
• Support periodic review activities related to Quality Operations.
• Conduct failure investigations and root cause analysis.
• Provide Internal audit and external audit support.
• Read and interpret drawings, QCIC's and test methods.
• Develop, prepare and report technical information to management to identify, segregate and disposition product through the nonconforming system.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
• Demonstrate independent understanding and application of core GMP fundamentals, including but not limited to: Data Integrity (DI), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDPs).
• Responsible for communicating business related issues or opportunities to next management level.
• Performs other duties assigned as needed.
EXPERIENCE
- High School Education or GED is required.
- 2-4 years of Medical Device Manufacturing Experience or related field.
SKILLS REQUIRED
Detail Attentive Awareness
Complaint Investigation Awareness
Data Capturing Awareness
Data Analysis Awareness
Root Cause Analysis (RCA) Awareness
Quality Focus Awareness
Quality Processes Awareness
Quality Assurance (QA) Awareness
Data Collection Awareness
Daya Gracia
Technical Recruiter-Life Science
Mobile/Text: 325-735-5606
3242 Executive Dr. | San Angelo, Texas 76905
Email: dayanara.gracia@bepcinc.com
www.bepcinc.com
https://www.linkedin.com/in/daya-gracia/
BEPC has an open position for a Translation Project Manager!
Contract W2 Period: 6-month contract with possibilities for extensions.
Pay & Benefits: $138-$170/hr. + Medical, Dental, Vision and Life Insurance
Candidate can be remote but if local can be onsite. will be working PST hours.
Position Summary
Experience Operations (XO) is a functional group within Genentech Business Operations (GBO) comprised of experts who partner across Commercial, Medical Affairs and Government Affairs (CMG) to orchestrate and deliver integrated customer experiences that drive measurable business outcomes.
In this position, the candidate will facilitate the day-to-day operations of our translation projects, working closely with the Translation Program Manager and coordinating with translation vendors. Their responsibilities will include receiving and processing translation requests, preparing materials for translation, managing communications between linguists, the content owners, and internal reviewers, and ensuring timely project delivery.
Additionally, the candidate will assist in tracking and reporting key performance metrics related to translation projects, collaborating with stakeholders to optimize processes and drive continuous improvement. They will work cross-functionally with a variety of stakeholders.
Key Responsibilities
Receive and process translation requests from internal content owners.
Prepare source and reference materials for translation following a standardized process, ensuring clarity and completeness.
Manage questions and clarifications from linguists and the translation team, acting as a bridge between them and content owners.
Interact with internal linguistic reviewers to gather feedback on the quality of translations provided by the vendor.
Create and maintain a translation project schedule, ensuring deadlines are met and resources are allocated efficiently, and escalating resourcing and priority conflicts for management support.
Update stakeholders on the status of translation projects, including progress and any potential delays.
Coordinate the submission of translated materials for regulatory review and approval, ensuring compliance with relevant guidelines and regulations.
Collaborate with vendors to ensure accurate and culturally appropriate translations.
Collaborate with vendors and internal linguistic reviewers to develop and improve linguistic assets (glossaries and style guides).
Maintain documentation and records related to translation projects and the linguistic decisions made.
Continuously evaluate and make recommendations to improve translation processes to optimize efficiency and quality.
Assist with tracking and reporting key performance metrics related to translation projects, including turnaround time, quality metrics, and vendor performance, to provide insights for process improvement and decision-making.
Skills & Competencies
Familiarity with translation industry standards, terminology, and best practices.
Strong organizational skills with the ability to effectively prioritize tasks and manage multiple projects simultaneously.
Excellent communication skills, both written and verbal, with the ability to interact professionally with internal stakeholders and external vendors.
Attention to detail and a commitment to ensuring accuracy and consistency in translated materials.
Proficiency in project management tools and software for scheduling, tracking, and reporting translation projects.
Ability to work collaboratively in a cross-functional team environment, fostering positive relationships and driving results.
Analytical mindset with the ability to inform decision-making and process improvements.
Problem-solving skills and the ability to proactively address challenges and mitigate risks throughout the translation process.
Qualifications & Experience - Required
Bachelor's degree in a related field such as Linguistics, Translation, Communications, other equivalent credential, or equivalent work experience.
A minimum of 2 years of experience managing translation projects in a professional setting, demonstrating proficiency in coordinating project timelines, resources, and deliverables.
Excellent communication skills, both written and verbal, with the ability to interact professionally with internal stakeholders and external vendors.
Familiarity with the management of translation quality using linguistic assets such as translation memories, glossaries/termbases, and style guides, ensuring consistency and adherence to brand guidelines.
Experience in linguistic review processes, including the ability to gather feedback from internal linguistic reviewers and effectively communicate revisions to translation vendors.
Familiarity with translation management systems (TMS).
Knowledge of industry-standard file formats and localization best practices for various content types, including print and digital documents, multimedia, and web content.
Demonstrated problem-solving abilities and the capacity to adapt to evolving project requirements and stakeholder expectations.
Qualifications & Experience - Preferred
Experience using JIRA or other project management software to effectively plan, track, and coordinate translation projects.
Fluency in Spanish.
Proficiency in additional languages.
BEOCS
BEPC has an open position for an Associate Systems Engineer in Tucson, AZ!!
Contract W2 Period: 18-month contract with possibilities for extensions.
Pay & Benefits: $33-$39/hr. + Medical, Dental, Vision and Life Insurance
Applies intensive and diversified knowledge of design principles, practices and implementation in complex systems and assignments. General responsibilities include design concept generation, participating in design reviews, development and testing to assess performance against design specification, reliability testing, and assessment of system interactions.
Makes independent decisions. Assist in the development of manufacturing processes and troubleshooting issues to determine root cause and possible engineering solutions.
Responsibilities
BEPC is looking for a Global Organic Mobile Acquisition QA Manager in Newark, NJ to join our fast-growing team of consultants!
W2 Contract: 9 months with opportunities for extensions based on business needs and performance.
**Hybrid Position in Newark, NJ**
Pay Range: $57.69-86.35/hr. plus we offer Medical, Dental, Vision and Life Insurance benefits!
About This Role:
The Global App Growth Marketing team is looking for a QA Manager to assist with the coordination and quality assurance of A/B tests in support of our global non-member program. This person will be the primary Q/A support across our global markets for the in-app testing program and have the opportunity to work with marketers to provide best in class experiences for our users and to enhance our acquisition efforts.
The role requires a keen sense of detail, 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.
Responsibilities:
BEPC is hiring a Facilities Project Engineer - Construction Safety Support in San Angelo TX
W2 1 year contract with potential for extension.
Job Overview:
EHS issues associated with facility and process equipment construction range from managing permits appropriately to assessing building materials to accurately understand the hazards. Appropriate identification and definition of these issues can reduce the potential for cost growth during the construction process and/or risks of potential non-compliance and subsequent government issued fines.
Experience should include facility construction experience and capital project support for the ETO Abatement Project in San Angelo, TX. Support is anticipated throughout the life cycle of a project. We are seeking proposals from companies that have a proven record of promoting effective planning, safe work execution, driving regulatory compliance, and preventing project cost and schedule creep.
Must have proven experience:
• Projects portfolio management.
• At least $3MM Capital projects per year
• Knowledge of key facilities process:
- Basic: Compressed air, Chillers, Boilers, Clean area, Fire System,
- Wish: Sterilization, Nitrogen plant, purification water plant
• Experience:
- Basic: PMO training, problem solving, Budget management
- Wish: PMI certificate, black belt training, procurement experience
The role of the construction safety DRI will be, but not limited to, as follows:
• Routinely monitor the contractor’s EHS performance to verify that the Contractor is in compliance with their stated practices and procedures, regulatory requirements and any additional owner expectations/deliverables that may have been identified in the contract of work EHS Schedule.
• Interface with and support the construction management team at the site by delivering current data on contractor EHS performance, including: trending, incident management, EHS metrics, and other key information that enable construction management to make informed and timely decisions.
• Facilitate communications, including safety meetings and notices, to ensure relevant EHS information is communicated across the site by contractors and that management is included in those communications.
• Conduct a weekly site safety walk with the contractor management representative.
• Participate in a daily site safety walk with the contractor safety rep.
• Act as a coach and advisor to the contractor safety committee.
• Evaluate the completeness and effectiveness of the contractor’s hazard assessments (JHAs, Good Saves etc.).
• When non-compliance and/or non-conformance is observed, immediately bring the issue to the attention of that individual and key stakeholders as appropriate.
• Verify key performance indices (KPIs), leading/lagging indicators, and EHS data submitted by the contractor are accurate, timely and complete.
• Conduct the monthly contractor EHS audit.
• Participate in progress and schedule meetings.
• Assist in design reviews throughout the Life Cycle-planning, as requested/required (design, permitting, construction, cx, handover, etc.).
• Attend client trainings as requested.
• Evaluate/audit Site Specific Safety Plan to conformance to Project Manual requirements.
• Understand and verify operational EHS requirements are adhered to.
• Support client initiatives as requested.
SCOPE OF WORK
Support the ETO Abatement Project San Angelo, TX site. The project is expected to begin in June 2020 and terminate in July 2021. We anticipate the scope of work will be conducted primarily by an experienced construction safety consultant. We will assist in the day-to-day application of EHS/CSS program including inspections, safety and compliance walks, root-cause analysis, and contractor review. Construction work will be scheduled for day shift.
Proposed 40 hours per week will be primarily focused to construction safety. Onsite work is expected to be 5 days per week on average.
BEOCS
Requirements:
Additional Requirements:
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 systems support a wide range of commercial and military platforms, including the burgeoning electric aviation market.
MINIMUM JOB REQUIREMENTS:
The Manufacturing Test Engineer develops and/or specifies necessary test equipment, software, and procedures for high volume production and testing of goods. This role develops and maintains test software, technical specifications and documentation for such equipment per established methods and also develops documentation and procedures as necessary for employee training and ISO compliance. This individual will work closely with other Engineering and Manufacturing personnel and provide assistance as needed for implementing test systems into production. The Manufacturing Test Engineer will also assist with operation, maintenance, validation, troubleshooting, and repair of test equipment.
Mfg Test Engineer Primary Responsibilities:
- Setup, troubleshoot and maintain test systems for production lines with good problem solving skills. Plan and execute continuous improvement the test solutions along the product lifecycle.
- Test system verification, validation and document maintenance to guarantee compliance for ISO and regulation requirements
- Contribute to the NPI decision on manufacturing test strategy and design the implementation plan
- Develop test methodology and design automated test systems to achieve quality and productivity goals for NPI and current process improvement
- Partner with a global R&D and NPI project team to plan, execute and coordinate new product releases.
- Create and support productivity tools, manufacturing data system and automated workflow to enhance cross-organization business efficiency
Basic Qualifications:
The job candidate must have a Bachelors or Master's Degree in Engineering disciplines, preferably Electrical Engineering, Computer Engineering, Computer Science, or Software Engineering with experience in the following areas:
Required skills:
- Hands-on experience of test system development and software program development.
- Programming skills required in some of the following languages: C-Family (C, C++, Java, C#), HTML, Visual Basic, Python, NI (LabView, TestStand).
- Demonstrated proficiency of system design for test hardware or software with disciplined DFx and FMEA principles and methodologies
- Demonstrates the abilities to produce useful engineering solutions for assigned problems in an independent manner.
- Demonstrated ability to set priorities and meet commitments.
- Ability to communicate needs, plans and achievements at all levels of a corporate organization.
- Ability to simultaneously participate in multiple issues as they arise in a manufacturing environment.
- Willingness to work in a hands-on environment.
- Willingness to take on new challenges and learn from the experience of coworkers. - - - Six Sigma Green belt certification
- Fluent in English and local dialect
BEOCS
BEPC is seeking a Software Engineer located in Phoenix, AZ!
Contract W2 Period: TBD
Description of the job:
BEPC Inc. is searching for an Advanced Manufacturing Engineer in Clearwater, FL.
CONTRACT W2: 6 – month contract with possibilities for extensions.
PAY AND BENEFITS: $29.00 – 33.00/HR. + medical, dental, vision and life insurance.
8 a.m. – 5 p.m.
Responsibilities:
Plans and designs manufacturing processes in industrial plant. Maximizes efficiency by analyzing layout of equipment, workflow, assembly methods, and work force utilization. Determines parts and tools needed to achieve manufacturing goals according to product specification. 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.
Experience:
May require a bachelor's degree in engineering and 0-2 years of experience in the field or in a related area.
BEPRO
BEPC Inc. Engineer II, Iriving Texas
Job Title: Engineer II
Location: Irving, TX
Job Function: Engineering
Select Exemption Status: Non-Exempt
SECTION 1: JOB SUMMARY*
? Responsible to identify process improvement initiatives and develops proposals for problem solving,
improvement or optimization.
? Support process improvement projects that have the objectives of developing more cost efficient and quality
enhanced processes.
? Establish machine and process standards and overall equipment efficiency.
? Assist in the development of more effective operational control systems.
? Evaluate data generated through studies using statistical analytical methods.
? Responsible for the development and/or revision of production standards and standard work documents.
? Develops, writes and executes engineering studies, design of experiments, and IQ/OQ/PQ protocols and
reports.
SECTION 2: DUTIES & RESPONSIBILITIES*
Under general direction and in accordance with all applicable federal, state and local laws/regulations and
Corporate Johnson & Johnson, procedures and guidelines, this position:
? Works on optimization of process output and throughput, equipment utilization, equipment downtime, waste
reduction/yield improvements, budget management, standard cost and capital investment management.
? Provides technical support to the production areas evaluating process deficiencies, process changes,
modifications and equipment failure. Defines, analyzes, reviews and evaluates problems for prompt solutions.
? Determines, adapts, and modifies methods and standards to control all aspects of assigned projects or portions of
major projects.
? Coordinates phases of work with other departments within the company and with other Medical Device divisions.
? Perform Investigation and writes NC reports following established timelines.
? Routes and follows up on NC reports through the evaluation, review and approval processes to comply with the
established timeline.
? Coordinates and participates in Cross Functional Investigations (CFI)
? Revise and maintain engineering and equipment procedures.
? Follows Standard Operating Procedures (SOP), Good Manufacturing Practices (GMPs), Company Policies and
Federal, State and Local Government Regulations.
? Map processes and analyze current status and potential future states with improvements. Define and quantify
improvements to further analyze the gains. Use tools from Lean and Six Sigma to create and execute CIP projects.
? Participates in GMP audits regarding equipment recording and machine performance.
? Coordinates communications and interfaces with end users, machine manufacturers and/or suppliers.
? Participates in projects involving other departments and activities (CIM, QIP, CFM, etc.).
? Writes, develops and implements validation procedures.
Comply J&J Safety Requirements and ensure safe working conditions and practices in the department.
? Reviews and analyzes data, understanding of statistics and the application of statistical data, able to determine
normal and non-normal data along with probable causes of non-normal results.
? Demonstrate independent understanding and application of core GMP fundamentals, including but not limited to:
Data Integrity (DI), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDPs).
? Responsible for communicating business related issues or opportunities to next management level
? Responsible for ensuring personal and Company compliance with all Federal, State, local and Company
regulations, policies, and procedures
? Performs other duties assigned as needed
SECTION 3: EXPERIENCE AND EDUCATION*
? Bachelor’s degree in engineering discipline.
? 2-4 years’ experience in engineering in a medical device environment preferred.
SECTION 4: REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and
AFFILIATIONS*
? Advanced computer skills and use of software applications. Strong computer background (MS Office, MS Project
Management, PowerPoint, Word, Excel, Outlook etc.)
? Experience in a manufacturing environment developing manufacturing standards.
? Proven ability to anticipate and solve problems.
? Ability to prioritize multiple commitments and technical problem-solving duties.
? Experience or knowledge in short and long-term project management.
? Advanced computer skills and use of software applications. Strong computer background (MS Office, MS Project
Management, PowerPoint, Word, Excel, Outlook etc.).
? Provides technical support to the production areas evaluating process deficiencies, process changes, modifications
and equipment failure. Defines, analyzes, reviews and evaluates problems for prompt solutions.
BEPC is actively looking for an Enviornmental Cleaning Specialist in the Sturgis, MI area!
12 month contract with possible extension
Benefits: Medical, Dental, Vision, and life insurance
Pay Rate: $15 - $17.16
Shift: 7:20AM - 3:50PM
EPC is actively looking for Production Worker 1 in the Altavista, VA area!
1 year contract with possible extension!
Benefits Medical, Dental, Vision, and Life Insurance
Pay Rate: $12.00-$14.30
Shift: 10:00pm - 6:30am
Hours over 40 will be paid at Time and a Half.
Job Duties:
BEPC is actively looking for Production Worker 1 in the Altavista, VA area!
1 year contract with possible extension!
Benefits Medical, Dental, Vision, and Life Insurance
Pay Rate: $12.00-$14.30
Shift: 6:30AM - 7:00PM
Hours over 40 will be paid at Time and a Half.
Job Duties:
BEPC has an open position for a M&E Event Planner
Location: Alpharetta, GA (up to 30% Travel)
Benefits: Medical, Dental, Vision, and Life Insurance
Pay Rate: $33.00 - $36.00 Per Hour
Shift: Monday – Friday 8 AM - 5 PM
Term: 6-Month Contract with possible extensions (Based on Performance)
Requirements: 5 years experience in Event Planning & CVENT + 4 year Degree.
**Position may require travel to domestic and international locations up to 30%. Potential site inspections and onsite execution of the event., Passport Required***
Job Description:
Function as primary client liaison and lead for assigned programs. Manage meetings and events through the implementation of strategy, delivery of objectives, and execution of logistics, while effectively working with multiple clients. Responsible for coordination of program planning from post-contract execution to final billing. Work closely with client contact to understand and meet program objectives/outcomes.
PROCESS MANAGEMENT:
BEPC is looking for an Associate Filling/Packaging Mechanic in Branchburg, NJ to join our fast-growing team of consultants!
W2 Contract: 6 months with opportunities for extensions based on business needs and performance.
Pay Range: $22.00-25.00/hr., depending on experience + we offer Medical, Dental, Vision and Life Insurance benefits!
Schedule: 100% Onsite, 7 a.m. – 3 p.m.
Job Summary:
Associate Filling/Packaging Mechanic responsibilities include setup and maintenance of automated filling and packaging equipment to ensure optimum operation and uptime. In addition, the Associate Filling/Packaging Mechanic must be able to effectively troubleshoot equipment, consulting with more experienced technicians.
Responsibilities:
BEPC Inc. searching for a Multi-Craft Maintenance Technician.
Who has 3 - 5 years minium experience working on production lines.
Prefer: On Medical devices.
Flexible must meet most of what is listed.
BEPC Inc.
BEPC is actively looking for a PV Clinical Scientist – ICSR in the South San Francisco, CA area!
Health Care Professional degree
5-month contract with possible extensions!
Benefits include medical, dental, vision, and life insurance
Pay Rate: $46.00-$50.00/hour
This position is remote, but the candidate should be in PST.
The PV Clinical Scientist - ICSR Case Management performs the tactical and operational job responsibilities, including but not limited to the collection, clinical review, evaluation, and processing of adverse event (AE) information received by US Patient Safety (USPS). The PV Clinical Scientist - ICSR Case Management performs clinical review of USPS cases (processed in-house or externally by the vendor) and supports the US Patient Safety PV Clinical Manager - ICSR Case Management in all activities. All responsibilities are performed under the direction of the PV Clinical Manager - ICSR Case Management.
Summary of Duties and Responsibilities:
• Completes patient safety monitoring and tracking in a timely, thorough, and accurate manner in accordance with pharmacovigilance (PV) and related standards, regulations Standard Operating Procedures (SOPs).
• Reviews, evaluates, and verifies potential AE information during triage to determine required action per internal policies and procedures and perform data entry of adverse event by timely completion of the case via safety database.
• Performs seriousness / validity/causality assessments and conducts quality review of all cases (as applicable) based on their medical assessment.
• Performs labeling assessment for AE(s) received using clinical knowledge and conducted follow up for all reported cases (as applicable).
• Responsible for Clinical Review of cases processed in-house and by vendors.
• Understands case processing data to evaluate error rates and potential compliance impact.
• Responsible for training internal USPS and/or vendors staff or team in collaboration with SP PV oversight based on trend analysis.
• Responsible for ensuring appropriate data correction in the safety database for identified issues or errors.
• Responsible for maintaining follow-up templates, ensuring successful transmission of all follow-up attempts performed by PV Clinical Scientist - ICSR Case Management/Vendor staff via the communication module.
• Accountable for training internal and external staff members on using communication module.
• Performs daily reconciliation of outgoing communications.
• Supports PV Clinical Scientist - Product in tasks and projects as needed.
• Responsible for identifying and developing training documents (i.e., SOPs) for the targeted audience (as needed).
• Assists in AE reconciliation activities and/or Case Transmission Verification (CTV) (as applicable)
• Acts as single point of contact with key stakeholders for safety-related activities, identifies potential business gaps and assists in the development and implementation of process solutions, and leads projects as assigned and under the direction of the US Patient Safety management.
• Responsible for the preparation and development of Patient Safety presentations and participates in the education offer internal /external stakeholders as applicable.
• Acts as Subject Matter Expert (SME) for safety-related activities within Global Safety Database per SOPs.
• Provide support during audits and inspections.
• Collaborates with PV Operations and SP PV Oversight teams as needed.
• Competencies Identified for Success:
• Demonstrates capability to comprehend medical information.
• Demonstrates ownership, initiative, and accountability.
• Sound decision-making abilities as demonstrated by systematic gathering of information, appropriately assessing the complexity of issues, and prioritization of tasks in a timely manner within the scope of responsibility.
• Ability to follow direction / guidance from USPS leadership or colleagues as required.
• Works well independent or within teams and is effective in collaborating with others internally and externally.
Qualifications:
• Health Care Professional degree (e.g., RN/BSN/MSN, NP, RPh/B Pharm/Pharm D, or MD) (Required)
• Minimum 5 - 7 years of clinical / Pharmacovigilance experience or 3 - 5 years with master’s or 0-2 years with PhD
• Writing experience; science/medical writing
• Communication and presentation skills; highly effective at summarizing and presenting key considerations and decision-points.
• Able to travel local / international as per business needs.
• Strong attention-to-detail
• Computer proficiency.
• Data entry experience.
• Project Management.
BEOCS
BEPC is looking for an Associate Dia Tech: Filling-1st Shift in Branchburg, NJ to join our fast-growing team of consultants!
W2-Contract: 6 months with opportunities for extensions based on business needs and performance.
Pay Range: $16.00-18.00/hr. plus we offer Medical, Dental, Vision and Life Insurance benefits!
Schedule: 100% Onsite, 7 a.m. 3:30 p.m.
Job Summary:
Performs duties related to filling, packaging, and warehousing of products (kits) containing various
components in accordance with industry standards and applicable regulatory requirements.
Responsibilities:
BEPC has an open position for a Material Handler in San Diego, CA!
Contract W2 Period: 12-Month contract with possibilities for extensions
Pay & Benefits: $17.00 - $19.00/hr. +Medical, Dental, Vision and Life Insurance
Shift: 7:30am - 4:00pm
REQUIREMENTS
• High school diploma.
Experience
Description:
Material Handler performs a full range of duties such as cycle counts, process of moving materials to departments and other facilities, performs general stock room activities, maintains Warehouse cleanliness, performs transactions in the ERP system, and ensures inventory counts are accurate.
Job Duties
BEPC has an open position for a Validation Engineer III in Oceanside, CA!!
Contract W2 Period: 8-month contract with possibilities for extensions.
Pay & Benefits: $68-$77/hr. + Medical, Dental, Vision and Life Insurance
Lead or support cleaning, equipment, utilities, sterilization and/or autoclave qualification due to equipment modifications for tech transfers, Make-Assess-Release (MAR) or routine re-qualification activities.
• Ensure the timely completion of Cleaning Monitoring as well as validation team assignments.
• Any deviations, anomalies or schedule impacting items are to be reported to site management.
• This position provides trained technical resources for the development and execution of validation protocols in accordance with OCN and global procedures. The person will maintain up-to-date training status in the Cornerstone (or equivalent) system.
• Author and review qualification protocols, engineering change orders, SOP changes, Engineering commissioning and turnover packages. Approval support of any qualification protocols will require approval of the site Validation as well as Quality.
• Review Planned/Unplanned events and provide initial assessment for validation lead.
• Review of lifecycle documents for migration into new electronic system as well as for additional changes for MAR, Tech transfer.
• Responsible for on-time completion of validation activities according to overall current manufacturing schedule.
• Ensure coordination of Validation requirements with Quality, Manufacturing & Engineering.
• Ensure the integration of environmental health, safety, and security into the business processes, systems and programs while reporting safety and environmental incidents including injuries, illnesses, and safety suggestions within one's functional area. Foster a positive safety culture in which no one gets hurt.
Additional
• This position provides resources for the controlled collection, assessment and reporting of scientific validation or study data in support of validation of processes.
The data will be analyzed using algebraic and/or statistical methods to verify adherence to predetermined and approved process criteria. Reports will be written to communicate the outcome of the studies and/or validations.
• This position will provide sampling and inspection support for process equipment as part of the validation execution process. As such, the person must be trained on sampling and inspection procedures; and may be called upon to provide training for others as needed.
Job Requirements
Education and Experience
• 5 -7 years of relevant validation engineer experience
• BA/BS in Engineering or Life Sciences
• Expert in current validation requirements and FDA expectation of facility, equipment, and computer validation.
• Establish and maintain good relationships with various site functional groups as well as external validation contractors and consultants.
• Ability to manage and track validation progress in required detail with data basis and
schedules.
• Excellent teamwork skills communication and problem-solving skills
• Good communication
Work Environment/Physical Demands/Safety Considerations
• Work in standard office environment.
• May on occasion work in clean room environment with large mechanical equipment, piping, and pumps connecting to tanks serviced by high-pressure steam, water and air together this creates a load environment.
• Maybe exposed to hazardous materials.
• Job descriptions are not intended, and should not be construed, to be all-inclusive lists of all responsibilities, skills, efforts, or working conditions associated with a job. While this description is intended to be an accurate reflection of the job requirements, management.
BEOCS
Responsibilities:
BEPC is actively looking for a Senior/Principal Scientist in Translational Medicine Mass Spectrometry in the South San Francisco, CA area!
PhD in Analytical Chemistry, Biochemistry, or Biotechnology and successful postdoctoral research training in a related field.
1 year contract with possible extensions!
Benefits include medical, dental, vision, and life insurance
Pay Rate: $95.00-$100.00/hour
Summary of Duties and Responsibilities:
• Informs clinical development of novel personalized therapeutics through establishment of biomarker strategies aimed to study biological pathways driving disease and by characterizing the mechanism of action of novel therapeutics.
• Utilize mass spectrometry to explore novel biomarker hypotheses, assist in streamlining existing workflows, and help to drive innovation within the group through improved LC-MS/MS method development.
• Experience in clinical proteomics and clinical sample processing is required.
• Hands-on experience with maintaining LC and MS instrumentation is also required.
• Perform other duties as required.
Qualifications:
• PhD in Analytical Chemistry, Biochemistry, or Biotechnology and successful postdoctoral research training in a related field
• Minimum of 6 years of hands-on experience with liquid chromatography and tandem mass spectrometry (LC-MS/MS) approaches and have excellent troubleshooting capabilities.
• Strong analytical background with fundamentals in assay development, system suitability, and method evaluation
• Experience with discovery proteomics approaches (TMT, DIA-MS, SWATH, etc.) and corresponding data analysis tools.
• Knowledge of sample preparation techniques for analysis of biomarkers and other mediators from biological fluids (e.g. plasma, CSF, urine, stool, etc.)
• Proven ability to analyze and visualize complex datasets using tools like MSstats, Spotfire, R, or Skyline and experience with standard instrument software such as Analyst or Xcalibur.
• Excellent communication, presentation, and interpersonal skills, be able to work independently as well as in a team environment and be willing and eager to learn and train others on new technologies.
BEOCS
BEPC is actively looking for Processing Operator III in the AltaVista, VA area!
5 month contract with possible extension!
Benefits: Medical, Dental, Vision, and Life Insurance.
Pay Rate: $13.00 - $16.55
Shift: 11:00 PM- 7:30 AM Mon. - Fri.
Job Duties:
In a production or manufacturing environment, the employee is responsible for:
BEPC is actively looking for an Operator 1 in Los Angeles, CA!
6-month contract with possible extension!
Benefits include medical, dental, vision, and life.
Pay Rate: $18.00 - $21.50
Shift: 7:30 am - 4:00 pm
Summary of Duties and Responsibilities:
- 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 GED required.
BEOCS
BEPC has an open position for a Validation Engineer III in Vacaville, CA!!
Contract W2 Period: 8-month contract with possibilities for extensions.
Pay & Benefits: $67-$81/hr. + Medical, Dental, Vision and Life Insurance
This is an onsite role; candidate should be local.
Primarily responsible for the support and execution of laboratory equipment qualification and
associated computer system validation activities in compliance with current cGMP regulations. You will work closely with instrument vendors, facilities, IT and lab personnel to coordinate the,
installation and the qualification including computer system validation, of QC Equipment Reader.
• Perform qualification of laboratory equipment in accordance with EQ policies, plans
and procedures.
• Coordinate with laboratory personnel to define qualification requirements.
• Author, review and execute equipment qualification protocols.
• Coordinate equipment qualification activities with vendors and other support
groups.
• Coordinate equipment maintenance activities with vendors and other support
groups, as required.
• Identify business, quality, and compliance gaps and propose and implement
potential improvements to systems and procedures
• Sign documents for activities as authorized and described by policies, procedures and job descriptions.
• Provide input to technical / investigation reports.
• Identify, troubleshoot, and propose resolution to technical problems.
• Receive and provide training.
• Provide input to and participate in assay transfer/validation associated with equipment qualification/lifecycle.
• Coordinate with customers to support multi-site operational activities.
• Present equipment lifecycle and associated procedures/material during internal and external audits and regulatory inspections.
• Works to meet schedules and set timelines.
• Perform other duties as requested by managers to support Quality activities.
Education:
• Bachelors degree (Life Science, Engineering)
Experience (may vary depending on site size/scope)
• Three to six years of validation experience (or equivalent experience) in a cGMP
environment with increasing levels of responsibility for a wide range of validation projects including validation of large-scale biochemical manufacturing, utility and automation systems.
BEOCS
BEPC has an open position for a Program Manager I in South San Francisco, CA!!
Contract W2 Period: 6-month contract with possibilities for extensions.
Pay & Benefits: $56-$66/hr. + Medical, Dental, Vision and Life Insurance
Bachelors Degree (life sciences or business discipline is preferred)
• Minimum of 2 years relevant work experience in the pharmaceutical/biotechnology industry
• Prior experience in product marketing, market or pipeline strategy, medical affairs or product development is preferred
• Good business acumen: possess knowledge of products and services provided by Roche/Genentech, and multidisciplinary functions involved in the drug development process
• Demonstrates some strategic agility and has the ability to identify new opportunities to streamline business processes and contribute to best practice
• Strong project and process management skills: can prioritize multiple tasks and goals to ensure they are on-time, on-target and within-budget
• Good communication (verbal, written) and presentation skills: can communicate in a timely, thorough, and concise manner and is comfortable presenting information to others at varying organizational levels
• Possess negotiation, interpersonal, and partnering skills: demonstrates some leadership skills, works well within teams, and is effective in collaborating with internal and external stakeholders
• Strong financial acumen: have proven abilities for effective planning, development, and oversight of project budgets and other resources
• Patient/customer focused
Physical work location: Open to onsite/hybrid/100% remote candidates should be in PST.
BEOCS
BEPC Inc. is searching for Drug Manufacturing Technician in Santa Rosa, CA.
W2 CONTRACT: 6 – month contract with possibilities for extensions.
PAY AND BENEFITS: $14.00 – 18.00 /hr. + Medical, Dental, Vision and Life Insurance.
** HOURS OVER 40 WILL BE PAID AT TIME AND A HALF**
9 a.m. – 5:30 p.m.
Job description:
JOB DESCRIPTION
This position is located in San Angelo, Texas.
Pay Rate: $14 - $16 per hour plus commission
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
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
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
Preferred Education and Experience
AAP/EEO Statement
BEPC Inc. policy is to affirmatively implement equal opportunity for all employees and applicants for employment without regard to race, color, religion, sex, national origin, disability, military status, genetic information, or any other basis prohibited by law. Additionally, BEPC Inc. does not discriminate against an employee or applicant who acts to oppose such discrimination or participates in the investigation of a complaint related to discriminatory employment practice. Employment decisions will be made on the basis of each applicant’s job qualifications, experience, and abilities.
BEOCS
Independent Contract QMS Auditor – North America
Requirements
The freelance Independent Contract Quality Management System (QMS) Auditor conducts supplier quality system audits, both on site and remote audits to applicable quality management system standards for Fortune 500 Medical Device Companies located in the North America. The independent contract auditor conducts audits of suppliers across different industries such as Medical device, Biotechnology, Microbiology and Sterilization Sciences as needed to meet customer requirements. The independent contract auditor must have the written and oral language skills to conduct supplier audits in English.
Competencies
BEPC is actively looking for a Environmental Cleaning Specialist in the Sturgis, MI area!
7-month contract with possible extensions!
Benefits include medical, dental, vision, and life
Pay Rate: $15.00-$18.03
Shift: 3:30pm-12:00am
Job Summary:
BEPC has an open position for an Instrument Technician II RDA-2nd Shift in Indianapolis, IN!!
Contract W2 Period: 24- month contract with possibilities for extensions.
Pay & Benefits: $25-$33/hr. + Medical, Dental, Vision and Life Insurance
Second Shift: 3:15 PM - 11:45 PM
Description:
The Off-Site Implementation Center (OSIC) Field Service Installation Technician will be responsible for the set-up and delivery of equipment ready for onsite installation at customer sites and according to the pre-installation process.
Set up and operate equipment and processes in accordance with standard operating procedures and site protocols.
Inspect product for quality and adherence to specifications.
Completes and ensures accuracy of all process orders and associated required documentation, records, and metrics.
Prepare and maintain work centers according to specifications.
May train others in the department as needed.
Responsible for maintaining and continuously improving the quality system and achieving quality objectives through daily actions.
Perform material handling of incoming and outgoing instruments.
Minimum Requirements:
High school diploma or GED and 2 years of technical school or equivalent military training or equivalent work experience
2 years progressive experience repairing or servicing mechanical/system hardware and software, or networking/wireless networking or equivalent military experience.
Effective time-management, organization and prioritization skills.
Good written/verbal communication skills
Detail oriented and ability to work in a fast-paced environment, both independently and within a team setting
Advanced knowledge of electronics, electro-mechanical systems, and information technology and/or certified Medical Technician
Valid forklift operator certificate or ability to obtain a forklift operator certificate.
Ability to understand and comply with appropriate safety, health, and environmental procedures.
Preferred Experiences:
Experience working in a Lean Manufacturing environment.
Experience working in a regulated work environment.
BEOCS
BEPC is actively looking for a Associate Manufacturing Operator in the Marana, AZ area!
11-month contract with possible extensions!!
Benefits include medical, dental, vison and life
Pay Rate: $15.00-$18.08
Schedule: Mon - Fri, 6:00 AM to 2:30 PM, Overtime Required
Summary:
The individual in this role contributes to producing reliable products and supplies with effective operations in an empowered organization. This contractor role is responsible for operating automated equipment and systems to perform a wide variety of tasks related to assembly, printing, fill and kitpack manufacturing operations.
Responsibilities:
- Executes the process of assembly, filling, labeling & packaging equipment of varying complexity and in accordance with production manufacturing records, operating procedure requirements to produce finished intermediates, instruments, and final kits while meeting production targets.
- Capable of basic transactions within highly complex systems and controls in a regulated manufacturing environment (e.g. receive, process, build product/materials, facilitate material availability, SAP transactions/confirmations).
- Contributes to daily end of shift reports and pass downs.
Safety and Quality
- Maintain Right to Operate and ensure that all processes are performed in a safe and healthy manner; Address and escalate any potentially unsafe hazards; Provides feedback during investigation of safety hazards, incidents and near misses using safety reporting tools.
- Perform tasks/transactions in the quality system to ensure we achieve our quality objectives.
- Understand the expectations of audit readiness (OSHA, FDA, QSR, GMP, ISO, etc.); may be required to answer questions about processes on the spot.
- Maintain accurate and complete system transactions ensuring material traceability, and inventory accuracy
(e.g. receipt, storage, issuance of materials, and other inventory transactions)
- Provide feedback on NCR investigations, reworks, and corrective actions.
- Adhere to 95% or above internal training compliance
- Responsible for 6S activities, gathering/meeting cycle times and developing/following standard work; identifies and implements process improvements and continuous improvement initiatives utilizing lean tools.
- Participates and contributes in shop floor tier meetings.
- Proactively collaborates with peers in other shifts/functions to ensure daily targets are achieved.
Other duties as assigned.
Education/Experience:
- High School Diploma/GED, required
- Associates Degree (preferred)
- 2 years relevant work experience, preferably in GMP environment
- Experience with automated manufacturing equipment in a regulated environment, preferred.
- Experience with validated software systems used to maintain Quality, Inventory, and Processes, preferred.
- Familiarity with sensors, motors, cylinders, etc., and with use of hand tools and test equipment, preferred.
Knowledge Skills and Abilities:
- Demonstrated experience with Lean / Continuous Improvement
- Experience with Google products (Gmail, gSheets, gDoc, etc), preferred
- Experience with SAP preferred
- Ability to read, write and comprehend English
- Ability to be agile and accurate in a high-volume environment
- Strong organizational skills, planning skills and attention to detail
- Strong communication skills - written, verbal
- Strong critical thinking, problem-solving and analytical skills
- Excellent time management skills to manage multiple tasks and daily production goals
- Ability to use the technology associated with the industry.
- Ability to use precision tools
- Ability to have prompt, regular and reliable worksite attendance.
BEOCS
BEPC is actively looking for a Business Engagement Coordinator!
Full-time position - Monday – Friday 8:00AM – 5:00PM
This position can be based in BEPC offices located in San Angelo Texas or Juarez, Mexico or can be a remote position with a stable internet connection to work in web enabled systems.
Reports to Supplier Auditing Account Manager /Division Director
JOB DESCRIPTION
Summary/Objective:
The Business Engagement Coordinator coordinates Supplier or External Manufacturer (EM) audits to company policies and procedures. This position ensures that the execution of the Supplier and External Manufacturers program is executed according to approved procedural requirements associated with fortune 500 Medical Device Companies.
Responsibilities:
• Supports the Supplier Audit department by maintaining the audit schedule in the Audit Resource Management System (ARMS) along with performing, filing, system maintenance and other duties.
• Enters supplier audit information into various systems, EtQ, SharePoint, ARMS and Curve.
• Maintains Supplier Audit files.
• Supports the incoming of the Request for Sourcing of new suppliers.
• Supports the program manager, and auditors as needed.
• Provides the supplier audit data and support department metrics and tracks improvements activities.
• Tracks progress of audits and provides status updates when required.
• Responsible for any other duties as assigned by the client for this role.
Other Duties:
Other duties may be assigned as required by BEPC management.
Competencies:
• Must be able to work independently, competent in use of a laptop computer and be proficient in Microsoft Office applications.
• Must be able to effectively speak, write and read in English.
• Excellent communication, well organized, and detail oriented are all necessary skills.
•Ability to build partnerships both internally and externally
• Must have a “Can do” attitude
• Must strive and be committed to “get the job done” and meet all deadlines
• Ability to learn and work using electronic web enabled systems
• Ability to multitask and consistently have attention to detail
• Must have the ability to respond to common inquiries or complaints from customers, or members of the business community.
• Basic understanding in FDA CFR Part 820, Part 11, and ISO 130485 regulations is required.
• Ability to stand firm while being open to new approaches.
• Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Routine Tasks:
• Creation and maintenance of EtQ audit records and supplier master records
• Creation and maintenance of Curve audit records
• Maintenance of ARMS data
• Management of refused audits
• Tracking required activities for refused audits, EAI audits, schedule changes, risk assessments, etc.
• Support activities related to ASL supplier additions, modifications and removals
• Support internal and external audits through supplier audit record investigation and retrieval.
• Support inquiries from audit scheduler, auditors and pre-audit teams
Supervisory Responsibility:
None
Work 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 with hours typically Monday – Friday 8AM – 5PM with some flexibility to work other hours as needed to meet with clients or auditors located in other time zones. This position can be based in BEPC offices located in San Angelo Texas or Juarez, Mexico or can be a remote position with a stable internet connection to work in web enabled systems.
Travel:
Minimal to no travel is required by this position.
Required Education and Experience:
• HS diploma or equivalent and a minimum of 7 years or bachelor’s degree and a minimum of 5 years of experience in a regulated industry such as medical devices are required.
• Knowledge of medical Device QSR's and ISO Standards 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.
BEOCS
BEPC is hiring a Validation Engineer in McKinney TX
Job Duration: 6 - 12 months with possible extensions
Looking for a strong validation engineer with quality engineering experience who is able to support validating activities at a Class I and Class 2 medical device manufacturing facility.
Experience with IQ/OQ/PQ validation protocols for medical device manufacturing
Upon successful IQ/OQ validations, author or support validation completion reports
Upon successful PQ validations, author or support validation completion reports
Provide technical expertise and support to generate and implement all associated Standard Operating Procedures newly validated medical device processes
At each phase of the validation process (from IQ through PQ), experience in trouble shooting, root cause analysis, problem solving, implementing effective corrective actions and following GMP requirements to ensure compliance to all medical device regulations
Capable and experienced in handling complex and highly technical processes
Able to effectively manage multiple detailed, complex validation
Capable of handling all aspects of validation work (creation of IQ, OQ, and PQ documents, etc..)
Job Requirements:
Degree in Engineering field (mechanical preferred) with upwards of 3-5 yrs. experience
General knowledge of medical devices is strongly preferred.
90% verbal English
Strong English written skills
Strong work ethic and demonstrates initiative
Proof of COVID vaccination required
BEOCS
BEPC Inc. is searching for a Production Technician in Houston, TX.
CONTRACT W2: 6 – month contract with possibilities for extensions.
PAY AND BENEFITS: $13.00 – 16.00/hr. + medical, dental, vision and life insurance.
** 6 a.m. – 4:30 p.m. **
HOURS OVER 40 WILL BE PAID AT TIME AND A HALF
Job responsibilities:
Production activities performed in a clean-room environment.
May be working with sophisticated equipment.
May require inspection of parts or product.
May be required to set up and/or monitor equipment at a basic level.
May be required to read, follow and maintain records.
May be required to maintain records according to Good Manufacturing Practices.
BEOCS
BEPC Inc.
Minimum of one year Contract
Benefits after 90 days
Come make a difference
Micro Biology Lab Tech & Analyst / Chemistry Lab Tech & Analyst
SECTION 1: JOB SUMMARY*
Responsible for conducting complex test and analysis to assure that product comply with established specifications.
SECTION 2: DUTIES & RESPONSIBILITIES*
Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate, procedures and guidelines, this position:
SECTION 3: EXPERIENCE AND EDUCATION*
Job Title |
Education |
Experience |
QC Lab Analyst I |
University/Bachelors Degree or Equivalent preferred |
Generally Requires 0-2 Years Work Experience |
QC Lab Analyst II |
University/Bachelors Degree or Equivalent preferred |
Generally Requires 2-4 Years Work Experience |
QC Lab Analyst III |
University/Bachelors Degree or Equivalent required |
Generally Requires 4-6 Years Work Experience |
QC Lab Analyst IV |
University/Bachelors Degree or Equivalent required |
Generally Requires 6-8 Years Work Experience |
KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS*
Call: Jesse Ramirez
BEPC Inc. Account Manager
325-315-2180
JOB DESCRIPTION
Summary/Objective
The Human Resources Partner handles and provides support for various HR employee programs within the organization. The primary responsibility is the performance of office work directly related to the general business operations of the business.
Responsibilities
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
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
Exempt
Travel
No travel is expected for this position.
Required Education and Experience
Preferred Education and Experience
BEOCS
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.
**Pay is based on experience and commission is offered**
BEPC is seeking 2 Dynamic Technical Recruiters to join our team at our headquarters location in San Angelo, TX
Technical Recruiter responsibilities include sourcing, screening and providing a shortlist of qualified candidates for various technical roles. You will also network online and offline with potential candidates to promote our employer brand, reduce our time-to-hire and ensure we attract the best professionals.
Ultimately, you will build a strong tech talent pipeline and help hire and retain skilled employees for our IT positions.
Responsibilities
Requirements
BEPC has an open position for a Remote Supplier Quality Compliance Engineer!
Pay & Benefits: $40/hr. + Medical, Dental, Vision and Life Insurance
BEPC has an open position for a Credit Investigator in Plano, TX!
Contract W2 Period: 6 month contract with possibilities for extensions
Pay & benefits: $19/hr. +Medical, Dental, Vision and Life Insurance
Required work hours: 8am – 7pm Monday – Sat.
There will be a variety of scheduling options within the 11 hours (i.e.: 8-5 PM, 9-6 PM, 10-7 PM, 11-8 PM, etc. with hour lunch) as each time zone will have flex shifts to cover high volume days, Monday and Saturday.
Job description:
In House Credit Investigation. To complete credit investigation for received credit applications
Must Haves:
BEPC Inc. is urgently seeking for a Shipping/ Receiving Clerk in Danbury, CT.
W2 CONTRACT PERIOD: 3-month contract with possibilities for extensions.
PAY AND BENEFITS: $17.50/ hr. + Medical, Dental, Vision and Life Insurance.
WORK HOURS: 10:00 a.m. – 7:00 p.m. M – F (5 – 10 hrs. a week in OT).
Job Description:
The key purpose of this function is to package product for daily and future shipment as per prescribed methods and/or to eliminate damage to product while in transit.
• Familiarity with carrier supplied Electronic Data Interchange systems.
• Must have good computer, written and communication skills.
• Shipping experience, a plus.
Essential Duties and Responsibilities:
The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.
• Package, process, inspect and transact all parcel orders.
• Generate required documents for shipment.
• Process documentation utilizing internal systems in addition to Electronic Data Interchange Systems supplied by various carriers.
• Prepares and packages products as per prescribed methods, verifying content against shipping and packaging documentation.
• Load and unload trucks.
• Responsible for storing packaging in its proper location.
• Maintain a safe and clean work environment.
• Palletize all out going product.
• Prepare consolidation orders for shipment.
• Prepare packaging for daily shipments.
• Ensure that skid dollies and brackets are returned to the vendor.
• Uncrate returned systems to be remanufactured.
• Respond to emails/calls and provide any information being requested in regards to shipping.
• Assists in maintaining packaging supply levels through inventory process.
• Processes customer orders utilizing carrier supplied systems and in-house systems.
• Actively supports and adheres to the Quality System, ISO 9001 principles and GMP’s.
The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Sit; use hands to finger, handle or feel objects, tools, or controls.
Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl.
Lifting/moving and carrying products weighing up to 50 pounds.
Exposure to moving mechanical parts, vibration and/or moderate noise levels.
Exposure to hazardous chemicals or other materials.
Safety shoes with impact and compression protection must be worn.
Education
• High School diploma or GED
BEOCS
BEPC Inc is seeking an Accounting SAP/ERP Analyst to join our fast growing team of consultants in the Plano, TX area!
Contract W2 Period: 6+ Months with opportunity for extensions
Pay & Benefits: $86.00/Hour + Medical,Dental,Vision & Life Insurance
Position Summary:
ERP - PeopleSoft is the current application supporting the General Ledger, Fixed Assets, Accounts Payable and Accounts Receivables. We have decided to replace PeopleSoft with SAP and update its downstream systems, deliverables, and business processes accordingly. Changes require updates to HFM, HFR Reports, and SmartView Spreadsheets.
This resource will act as a Functional Accounting Consultant for the Accounting Team for our ERP Project and will work closely with our General Manager Enterprise Systems (Project Leader) to develop accounting requirements, design and assist with system builds, testing, and deliverables implementation for our new ERP system. This individual will need to be strategic and forward thinking and understand the implications/impacts of an SAP Implementation on the Accounting Group.
This role is focused on GL Accounting and Financial reporting experience (more of a true accounting role). This person will be working closely with managers and directors.
Must Haves:
· CPA
· Bachelor’s degree
· General Accounting and Financial Reporting Experience
· SAP Implementation Experience
· Business Requirements gathering, understanding, and translating
· Must be able to work independently
· Excellent communication skills
· Influencing Customers and Users
Preferred/ Nice-to-haves:
· Consulting experience
· Business Process Transformation experience
· Agile/Scrum methodology experience
JOB DESCRIPTION:
Support the Government Pricing team in data prep, validation, and analytics related to Sandoz participation in the following government programs: Medicare Part B, VA Federal Supply Schedule Program, Medicaid Drug Rebate Program, and PHS 340B Drug Discount Program.
RESPONSIBILITIES:
Skills:
Preferred:
VALUES AND BEHAVIORS:
Education:
Minimum:
Skills and Experience:
Required Skills:
Additional Skills:
JOB DESCRIPTION - Technical Recruiter
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. 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
Competencies
Reports to Division Director
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.
Travel: No travel is expected for this position.
Required Education and Experience
Preferred Education and Experience
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.
Job Type: Full-time
BEOCS
Title: Finance Analyst (Salvacar)
Duration: 6 Months
Job Duties:
Description:
The candidate is responsible for the timely and accurate manufacturing of Bulk Pharmaceutical Chemicals (BPC’s) and Active Pharmaceutical Ingredients (API’s) regulated by the Food and Drug Administration following protocols consistent with, and established according to current Good Manufacturing Practices.
ESSENTIAL JOB FUNCTIONS
• Perform production operations per approved manufacturing procedures for release as BPC’s and API’s.
• Thoroughly document all production activities per FDA and cGMP guidelines.
• Perform and interpret analytical evaluation of BPC’s and API’s.
• Revise Master Manufacturing Formulas; Prepare and review Operating Procedures to ensure compliance with FDA and cGMP guidelines.
• Contribute to the support of the production operations for safety and compliance with FDA and cGMP guidelines.
• Develop and assist in the implementation of process improvement ideas.
• Assist in the training of Chemical Processors.
BASIC QUALIFICATIONS
Education: BS or BA in Chemistry, Biochemistry, Chemical Engineering, Biology or related life science
Essential and Critical Skills:
Knowledge in chemistry, biochemistry, math and general science.
Basic understanding of current Good Manufacturing Practices
Familiarity with analytical instruments and production equipment
Shiftwork is required
50 pound lifting required
Quality Engineer Sr.
Fully Bilingual
Validation Experience
Medical device experience background
Assist in operation and maintenance of Utility Operations equipment and systems.
Assist with timely completion of tasks and work orders with appropriate documentation according to standard operating procedures, applicable standards, guidelines, practices, and policies.
Safe operation of tools and shop equipment, and safe execution of work in the field.
Skills: Job Requirements:
Basic working knowledge of industrial equipment such as valves, pumps, motors, air compressors, and other Utilities related equipment.
Ability to complete tasks by following Standard Operating Procedures.
Ability to lift 50 pounds, and climb ladders.
Willingness to accept challenging assignments and tasks and completes same on time.
Ability to communicate clearly, both verbally and writing; and to maintain accurate documentation consistently.
Ability to perform administrative tasks with little supervision.
Basic computer skills, with the ability to utilize the corporate intranet and applications, and standard word processing and spreadsheet programs.
Keywords:
Education: High School Diploma required, and Machinist Mate or Boiler Technician experience
Tittle: Process Engineer
Duration- 12 months with the option to renew
Requirements