Associate, QC Analytical (Cell based assays, qPCR, Flow Cytometry)
Bristol Myers Squibb
August 29, 2026
Remote friendly (Devens, MA)
United States
Operations
Position: Associate, QC Analytical, Cell Therapy (3)
Schedule: Wed–Sat 2pm–12am
Position Summary:
Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts.
Key Responsibilities:
- Perform routine testing of in-process, final product, and stability samples.
- May review GMP documentation and perform data verification.
- Support document revision, project, CAPA, deviation/investigation, and/or continuous improvement efforts.
- May train analysts on general job duties.
- Perform other tasks as assigned.
Qualifications & Experience:
- Ability to accurately and completely understand and follow procedures.
- Apply scientific principles to analytical testing and proper use of laboratory equipment.
- Communicate effectively with peers and management regarding task completion, roadblocks, and needs.
- Attention to detail and demonstrated organizational skills.
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
Education/Experience/Licenses/Certifications:
- Bachelor’s degree preferred in science; equivalent Associate’s may be considered (Netherlands: Bachelor’s/HLO in bioanalytical science preferred; MLO level 4 may be considered).
- 0–2+ years relevant analytical testing or QC experience (preferably regulated environment).
- Demonstrated basic laboratory techniques and safety practices.
- Prior cell/molecular biology experience preferred (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique).
Compensation Overview (Devens, MA, US): $36.90–$44.71 per hour.
Schedule: Wed–Sat 2pm–12am
Position Summary:
Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts.
Key Responsibilities:
- Perform routine testing of in-process, final product, and stability samples.
- May review GMP documentation and perform data verification.
- Support document revision, project, CAPA, deviation/investigation, and/or continuous improvement efforts.
- May train analysts on general job duties.
- Perform other tasks as assigned.
Qualifications & Experience:
- Ability to accurately and completely understand and follow procedures.
- Apply scientific principles to analytical testing and proper use of laboratory equipment.
- Communicate effectively with peers and management regarding task completion, roadblocks, and needs.
- Attention to detail and demonstrated organizational skills.
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
Education/Experience/Licenses/Certifications:
- Bachelor’s degree preferred in science; equivalent Associate’s may be considered (Netherlands: Bachelor’s/HLO in bioanalytical science preferred; MLO level 4 may be considered).
- 0–2+ years relevant analytical testing or QC experience (preferably regulated environment).
- Demonstrated basic laboratory techniques and safety practices.
- Prior cell/molecular biology experience preferred (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique).
Compensation Overview (Devens, MA, US): $36.90–$44.71 per hour.