Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations
Bristol Myers Squibb
September 02, 2026
On-site
Summit, NJ
Operations
Shift Available (Onsite Day Shift): Quad 3: Wednesday–Saturday (with e/o Wednesday off), 5:00 a.m.–5:30 p.m. Times may change based on business demands.
Responsibilities:
- Set up and operate equipment to produce blood component lots through cell culture, harvest, and cryopreservation.
- Support deviation investigations and write-ups; support on-time closure of assigned CAPAs during shift.
- Perform aseptic tube activities (welding, connections, transfers); complete aseptic qualification.
- Weigh and measure in-process materials.
- Follow production schedule to ensure on-time internal production logistics.
- Record production data per GDPs.
- Execute work consistent with site safety, quality systems, and GMP.
- Work in a team cross-functionally to complete shift-required production tasks.
- Become a SME and qualified trainer in a designated manufacturing function; maintain training assignments on time.
- Perform other assigned tasks (e.g., continuous improvement, inspection readiness).
Knowledge & Skills:
- Basic cell culture, cryopreservation, purification, and aseptic processing/lab technique.
- cGMP/FDA-regulated industry knowledge; understanding of cGMPs.
- Basic math; technical writing; MS Office.
- Background understanding of biology, chemistry, medical/clinical practices.
Minimum Requirements:
- High School Diploma required; Bachelor’s/associate degree preferred.
- 0–1 years of cGMP cell therapy manufacturing/bioprocessing or relevant experience.
Working Conditions:
- Standing/walking/sitting; ability to stand extended periods.
- Work with contained human blood components; lift up to 25 lbs.
- Cleanroom PPE/garments required; no food or outside materials in restricted areas.
Benefits (as stated): Eligible for comprehensive benefits (medical/dental/vision/life/disability; wellbeing, retirement/financial protection). U.S. exempt: FTO plus 11 paid holidays; other groups per described vacation/holiday allowances.
Responsibilities:
- Set up and operate equipment to produce blood component lots through cell culture, harvest, and cryopreservation.
- Support deviation investigations and write-ups; support on-time closure of assigned CAPAs during shift.
- Perform aseptic tube activities (welding, connections, transfers); complete aseptic qualification.
- Weigh and measure in-process materials.
- Follow production schedule to ensure on-time internal production logistics.
- Record production data per GDPs.
- Execute work consistent with site safety, quality systems, and GMP.
- Work in a team cross-functionally to complete shift-required production tasks.
- Become a SME and qualified trainer in a designated manufacturing function; maintain training assignments on time.
- Perform other assigned tasks (e.g., continuous improvement, inspection readiness).
Knowledge & Skills:
- Basic cell culture, cryopreservation, purification, and aseptic processing/lab technique.
- cGMP/FDA-regulated industry knowledge; understanding of cGMPs.
- Basic math; technical writing; MS Office.
- Background understanding of biology, chemistry, medical/clinical practices.
Minimum Requirements:
- High School Diploma required; Bachelor’s/associate degree preferred.
- 0–1 years of cGMP cell therapy manufacturing/bioprocessing or relevant experience.
Working Conditions:
- Standing/walking/sitting; ability to stand extended periods.
- Work with contained human blood components; lift up to 25 lbs.
- Cleanroom PPE/garments required; no food or outside materials in restricted areas.
Benefits (as stated): Eligible for comprehensive benefits (medical/dental/vision/life/disability; wellbeing, retirement/financial protection). U.S. exempt: FTO plus 11 paid holidays; other groups per described vacation/holiday allowances.