Senior Specialist, QC Analytical, Cell Therapy A2 Shift
Bristol Myers Squibb
5 days ago
On-site
Devens, MA
Operations
Shift: A2 (Sunday–Wednesday, 2:00 PM–12:00 AM)
Position Summary:
Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts.
Key Responsibilities:
- Perform method transfer/validation and routine testing of in-process, final product, and stability samples.
- Anticipate and perform routine troubleshooting and problem solving with minimal guidance.
- Perform data verification, data review, and review of GMP documentation.
- Complete document revision, project, CAPA, and deviation/investigation tasks and/or continuous improvement.
- Train and mentor others on QC test methods, processes, and procedures.
Qualifications & Experience:
- Ability to understand, follow, interpret, and apply Global Regulatory and cGMP requirements.
- Demonstrated technical writing skills.
- High problem-solving ability; logical and technically adept.
- Effective communication with peers, management, and cross-functional partners.
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
- Advanced knowledge of LIMS/ELN and laboratory data analysis systems preferred.
- Bachelor’s degree (preferably science); Netherlands: Bachelor’s/HLO in (bioanalytical) science required.
- 4+ years relevant analytical testing/QC experience (preferably regulated environment).
- Cell & molecular biology experience (e.g., cell-based assays, flow cytometry, qPCR, ELISA, aseptic technique).
Compensation/Benefits:
- Devens, MA (US): $43.84–$53.12/hour. Additional incentive cash/stock may be available.
- Health coverage, wellbeing support, and financial wellbeing/protection (includes 401(k), disability, life insurance, etc.).
- Work-life benefits include Paid Time Off (details vary by location/employee type).
If a role intrigues you but doesn’t perfectly match your resume, you are encouraged to apply anyway.
Position Summary:
Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts.
Key Responsibilities:
- Perform method transfer/validation and routine testing of in-process, final product, and stability samples.
- Anticipate and perform routine troubleshooting and problem solving with minimal guidance.
- Perform data verification, data review, and review of GMP documentation.
- Complete document revision, project, CAPA, and deviation/investigation tasks and/or continuous improvement.
- Train and mentor others on QC test methods, processes, and procedures.
Qualifications & Experience:
- Ability to understand, follow, interpret, and apply Global Regulatory and cGMP requirements.
- Demonstrated technical writing skills.
- High problem-solving ability; logical and technically adept.
- Effective communication with peers, management, and cross-functional partners.
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
- Advanced knowledge of LIMS/ELN and laboratory data analysis systems preferred.
- Bachelor’s degree (preferably science); Netherlands: Bachelor’s/HLO in (bioanalytical) science required.
- 4+ years relevant analytical testing/QC experience (preferably regulated environment).
- Cell & molecular biology experience (e.g., cell-based assays, flow cytometry, qPCR, ELISA, aseptic technique).
Compensation/Benefits:
- Devens, MA (US): $43.84–$53.12/hour. Additional incentive cash/stock may be available.
- Health coverage, wellbeing support, and financial wellbeing/protection (includes 401(k), disability, life insurance, etc.).
- Work-life benefits include Paid Time Off (details vary by location/employee type).
If a role intrigues you but doesn’t perfectly match your resume, you are encouraged to apply anyway.