Technician, QC Sample Management, Cell Therapy
Bristol Myers Squibb
July 02, 2026
On-site
Devens, MA
Operations
QC Sample Management Technician
Shift/Hours
- 6PM–6AM on a 12-hour rotating shift (36/48 hours over a 2-week period); every other weekend and scheduled holidays; overtime as needed.
Responsibilities
- Handle QC test samples across receipt, storage, distribution, transfer, and disposal; facilitate cold-chain transfers.
- Ensure proper labeling; maintain sample tracking, labeling, and chain-of-custody records per regulatory requirements and written procedures.
- Maintain inventory and distribute QC samples/materials to functional groups as scheduled/requested.
- Record sample management performance metrics.
- Support process-efficiency identification and implementation.
- Communicate status, roadblocks, and needs to management.
Education
- Associate’s degree in Chemistry, Microbiology, or related science; or high school diploma/GED plus 2+ years relevant experience (preferably regulated). Equivalent education/experience may substitute.
Qualifications/Preferred
- Cold-chain sample storage/transfer experience in a GMP regulated environment (desirable).
- Basic electronic systems knowledge (email, MS Office).
- LIMS and ELN experience preferred.
- Able to lift/carry up to 20 lbs.
- GMP-related regulatory knowledge preferred; attention to detail and organizational skills.
- Ability to adapt to changing priorities/deadlines and work in a fast-paced team; effective communication.
Working Conditions
- Exposure to biohazardous materials and fluctuating/extreme temperatures.
Compensation & Benefits (as stated)
- Devens, MA: $27.35–$33.14 per hour (plus possible incentives).
- Health, wellbeing programs, and 401(k)/insurance benefits; paid time off per described eligibility.
Application
- Apply even if your resume doesn’t perfectly match the requirements.
Shift/Hours
- 6PM–6AM on a 12-hour rotating shift (36/48 hours over a 2-week period); every other weekend and scheduled holidays; overtime as needed.
Responsibilities
- Handle QC test samples across receipt, storage, distribution, transfer, and disposal; facilitate cold-chain transfers.
- Ensure proper labeling; maintain sample tracking, labeling, and chain-of-custody records per regulatory requirements and written procedures.
- Maintain inventory and distribute QC samples/materials to functional groups as scheduled/requested.
- Record sample management performance metrics.
- Support process-efficiency identification and implementation.
- Communicate status, roadblocks, and needs to management.
Education
- Associate’s degree in Chemistry, Microbiology, or related science; or high school diploma/GED plus 2+ years relevant experience (preferably regulated). Equivalent education/experience may substitute.
Qualifications/Preferred
- Cold-chain sample storage/transfer experience in a GMP regulated environment (desirable).
- Basic electronic systems knowledge (email, MS Office).
- LIMS and ELN experience preferred.
- Able to lift/carry up to 20 lbs.
- GMP-related regulatory knowledge preferred; attention to detail and organizational skills.
- Ability to adapt to changing priorities/deadlines and work in a fast-paced team; effective communication.
Working Conditions
- Exposure to biohazardous materials and fluctuating/extreme temperatures.
Compensation & Benefits (as stated)
- Devens, MA: $27.35–$33.14 per hour (plus possible incentives).
- Health, wellbeing programs, and 401(k)/insurance benefits; paid time off per described eligibility.
Application
- Apply even if your resume doesn’t perfectly match the requirements.