Associate, QC Microbiology, Cell Therapy (Wed-Saturday 2:00 p.m. to 12:00 a.m Shift)
Bristol Myers Squibb
August 06, 2026
Remote friendly (Devens, MA)
United States
Operations
Position Summary
- Support QC testing for in-process, final product, and stability samples; support environmental and facility monitoring.
- May assist with documentation, deviations, investigations, and continuous improvement efforts.
Shift Details
- Wednesday–Saturday, 2:00 p.m. to 12:00 a.m.
Duties/Responsibilities
- Perform routine testing of in-process, final product, and stability samples.
- Perform environmental/facilities monitoring and microbiological testing.
- Review GMP documentation; perform data verification.
- Support document revision; CAPA and deviation/investigation tasks; continuous improvement.
- May train analysts on general job duties.
- Perform other tasks as assigned.
Reporting Relationship
- Reports to QC management.
Qualifications
- Ability to follow procedures accurately and completely.
- Apply scientific principles to QC testing and proper use of laboratory equipment.
- Communicate effectively with peers and management.
- Attention to detail and organizational skills.
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize.
Education/Experience
- Bachelor’s degree preferred in science; associate degree with equivalent education/work experience considered.
- 0–2+ years relevant microbiological testing or QC experience (preferably regulated environment).
- Demonstrated basic laboratory techniques and safety practices; prior microbiological techniques preferred.
Benefits (explicit)
- Health coverage (medical, pharmacy, dental, vision); wellbeing support; 401(k) and insurance/disability.
- Paid time off (role-dependent) and additional eligible time off programs.
Application instructions
- Apply even if the resume doesn’t fully match.
- Support QC testing for in-process, final product, and stability samples; support environmental and facility monitoring.
- May assist with documentation, deviations, investigations, and continuous improvement efforts.
Shift Details
- Wednesday–Saturday, 2:00 p.m. to 12:00 a.m.
Duties/Responsibilities
- Perform routine testing of in-process, final product, and stability samples.
- Perform environmental/facilities monitoring and microbiological testing.
- Review GMP documentation; perform data verification.
- Support document revision; CAPA and deviation/investigation tasks; continuous improvement.
- May train analysts on general job duties.
- Perform other tasks as assigned.
Reporting Relationship
- Reports to QC management.
Qualifications
- Ability to follow procedures accurately and completely.
- Apply scientific principles to QC testing and proper use of laboratory equipment.
- Communicate effectively with peers and management.
- Attention to detail and organizational skills.
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize.
Education/Experience
- Bachelor’s degree preferred in science; associate degree with equivalent education/work experience considered.
- 0–2+ years relevant microbiological testing or QC experience (preferably regulated environment).
- Demonstrated basic laboratory techniques and safety practices; prior microbiological techniques preferred.
Benefits (explicit)
- Health coverage (medical, pharmacy, dental, vision); wellbeing support; 401(k) and insurance/disability.
- Paid time off (role-dependent) and additional eligible time off programs.
Application instructions
- Apply even if the resume doesn’t fully match.