Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations
Bristol Myers Squibb
September 03, 2026
On-site
Summit, NJ
Operations
Role Statement
- Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under supervision of Manufacturing Management.
- Communicate production deviations and assist with quality investigations as applicable.
Shift Available
- Quad 4: Wednesday–Saturday (with every other Wednesday off), onsite overnight 5:00 p.m.–5:30 a.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/write-ups and timely closure of assigned CAPAs within the shift.
- Perform aseptic technique for tube-most activities (welding, connections, transfers); maintain aseptic qualification.
- Weigh and measure in-process materials.
- Follow production schedule and internal production logistics.
- Record production data per GDPs.
- Perform tasks consistent with site safety, quality systems, and GMP requirements.
- Work in a team-based, cross-functional environment.
- Become a SME and qualified trainer within a designated manufacturing function.
- Maintain on-time completion of training assignments.
- Other assigned tasks (continuous improvement, inspection readiness, right-first-time).
Knowledge & Skills
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing/lab technique.
- Knowledge of cGMP/FDA regulated industry and general understanding of cGMPs.
- Basic math, technical writing, MS Office.
- Understanding of biology, chemistry, medical or clinical practices.
Basic Requirements
- Minimum high school diploma/equivalent; associate/bachelor’s preferred.
- 0–1 year of cGMP cell therapy manufacturing/bioprocessing manufacturing or relevant experience/education.
Working Conditions
- Walk/stand/sit; may require standing for extended periods; lift up to 25 lbs.
- Work with contained human blood components in laboratories and controlled enclosed restricted areas.
- Use required cleanroom garments and PPE; restricted areas prohibit food and outside materials (e.g., cell phones, tablets).
- Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under supervision of Manufacturing Management.
- Communicate production deviations and assist with quality investigations as applicable.
Shift Available
- Quad 4: Wednesday–Saturday (with every other Wednesday off), onsite overnight 5:00 p.m.–5:30 a.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/write-ups and timely closure of assigned CAPAs within the shift.
- Perform aseptic technique for tube-most activities (welding, connections, transfers); maintain aseptic qualification.
- Weigh and measure in-process materials.
- Follow production schedule and internal production logistics.
- Record production data per GDPs.
- Perform tasks consistent with site safety, quality systems, and GMP requirements.
- Work in a team-based, cross-functional environment.
- Become a SME and qualified trainer within a designated manufacturing function.
- Maintain on-time completion of training assignments.
- Other assigned tasks (continuous improvement, inspection readiness, right-first-time).
Knowledge & Skills
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing/lab technique.
- Knowledge of cGMP/FDA regulated industry and general understanding of cGMPs.
- Basic math, technical writing, MS Office.
- Understanding of biology, chemistry, medical or clinical practices.
Basic Requirements
- Minimum high school diploma/equivalent; associate/bachelor’s preferred.
- 0–1 year of cGMP cell therapy manufacturing/bioprocessing manufacturing or relevant experience/education.
Working Conditions
- Walk/stand/sit; may require standing for extended periods; lift up to 25 lbs.
- Work with contained human blood components in laboratories and controlled enclosed restricted areas.
- Use required cleanroom garments and PPE; restricted areas prohibit food and outside materials (e.g., cell phones, tablets).