Specialist, QC Analytical Molecular B2 Shift, Cell Therapy
Bristol Myers Squibb
August 24, 2026
Remote friendly (Devens, MA)
United States
Operations
Responsibilities:
- Perform routine testing of in-process, final product, and stability samples.
- Perform testing for method transfer/validation/verification.
- Perform data verification, data review, and review of GMP documentation for general methods.
- May perform document revision; project work; CAPA; and deviation/investigation and/or continuous improvement tasks.
- Train analysts on general job duties.
- Perform other tasks as assigned.
Shift:
- B2 (2pm–12am, Wednesday–Saturday).
Qualifications/Requirements:
- Ability to accurately understand, follow, interpret, and apply Global Regulatory and cGMP requirements.
- Bachelor’s degree (or equivalent), preferably in science (Netherlands: Bachelor’s degree/HLO in bioanalytical science preferred; MLO level 4 with equivalent experience may be considered).
Preferred Skills/Experience:
- Knowledge of LIMS and ELN; laboratory data analysis systems.
- Problem-solving ability; technically adept and logical.
- Effective communication with peers and cross-functional partners.
- Experience with writing technical documents.
- Ability to work in a fast-paced team, meet deadlines, and prioritize work.
Compensation/Benefits (as stated):
- Devens, MA (US): $40.04–$48.52/hour.
- Health coverage; wellbeing support; 401(k); disability and life insurance (eligibility/enrollment may be required).
Application instruction (as stated):
- If the role doesn’t perfectly match your resume, apply anyway.
- Perform routine testing of in-process, final product, and stability samples.
- Perform testing for method transfer/validation/verification.
- Perform data verification, data review, and review of GMP documentation for general methods.
- May perform document revision; project work; CAPA; and deviation/investigation and/or continuous improvement tasks.
- Train analysts on general job duties.
- Perform other tasks as assigned.
Shift:
- B2 (2pm–12am, Wednesday–Saturday).
Qualifications/Requirements:
- Ability to accurately understand, follow, interpret, and apply Global Regulatory and cGMP requirements.
- Bachelor’s degree (or equivalent), preferably in science (Netherlands: Bachelor’s degree/HLO in bioanalytical science preferred; MLO level 4 with equivalent experience may be considered).
Preferred Skills/Experience:
- Knowledge of LIMS and ELN; laboratory data analysis systems.
- Problem-solving ability; technically adept and logical.
- Effective communication with peers and cross-functional partners.
- Experience with writing technical documents.
- Ability to work in a fast-paced team, meet deadlines, and prioritize work.
Compensation/Benefits (as stated):
- Devens, MA (US): $40.04–$48.52/hour.
- Health coverage; wellbeing support; 401(k); disability and life insurance (eligibility/enrollment may be required).
Application instruction (as stated):
- If the role doesn’t perfectly match your resume, apply anyway.