Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations
Bristol Myers Squibb
September 02, 2026
On-site
Summit, NJ
Operations
Duties/Responsibilities:
- Perform set-up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.
- Support deviation investigations and write-ups.
- Support on-time closure of assigned CAPAs within the designated shift.
- Perform aseptic tube most activities (welding, connections, transfers); aseptic qualification required.
- Weigh and measure in-process materials to ensure correct quantities are added/removed.
- Adhere to the production schedule and internal production logistics.
- Record production data/information clearly and concisely according to GDPs.
- Perform tasks consistent with site safety policies, quality systems, and GMP requirements.
- Work in a team-based, cross-functional environment to complete shift-required production tasks.
- Become an SME and qualified trainer within a designated manufacturing function; maintain on-time completion of training assignments.
Reporting Relationship:
- Reports to the Manufacturing Manager. (Supervision by shift Supervisor or designated Team Lead.)
Qualifications / Knowledge, Skills, and Abilities:
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing/lab technique.
- Knowledge of cGMP/FDA regulated industry.
- Basic mathematical skills; general understanding of cGMPs.
- Technical writing capability.
- Proficient in MS Office.
- Background understanding of biology, chemistry, medical, or clinical practices.
- Prior experience in Manufacturing and/or scientific/engineering education.
Education:
- Bachelor’s degree; or Associate/Medical Technical degree with 3 years of Manufacturing; or Operations experience.
- High School diploma/GED with 2 years of Manufacturing or Operations experience.
- Perform set-up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.
- Support deviation investigations and write-ups.
- Support on-time closure of assigned CAPAs within the designated shift.
- Perform aseptic tube most activities (welding, connections, transfers); aseptic qualification required.
- Weigh and measure in-process materials to ensure correct quantities are added/removed.
- Adhere to the production schedule and internal production logistics.
- Record production data/information clearly and concisely according to GDPs.
- Perform tasks consistent with site safety policies, quality systems, and GMP requirements.
- Work in a team-based, cross-functional environment to complete shift-required production tasks.
- Become an SME and qualified trainer within a designated manufacturing function; maintain on-time completion of training assignments.
Reporting Relationship:
- Reports to the Manufacturing Manager. (Supervision by shift Supervisor or designated Team Lead.)
Qualifications / Knowledge, Skills, and Abilities:
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing/lab technique.
- Knowledge of cGMP/FDA regulated industry.
- Basic mathematical skills; general understanding of cGMPs.
- Technical writing capability.
- Proficient in MS Office.
- Background understanding of biology, chemistry, medical, or clinical practices.
- Prior experience in Manufacturing and/or scientific/engineering education.
Education:
- Bachelor’s degree; or Associate/Medical Technical degree with 3 years of Manufacturing; or Operations experience.
- High School diploma/GED with 2 years of Manufacturing or Operations experience.