CAR-T Cell Therapy Manufacturing Associate

Bristol Myers Squibb EU Policy; West Summit (UT); On-site; USD 79,744,000 - 96,622,000; Full time

Job summary

Bristol Myers Squibb is seeking a Manufacturing Associate to produce blood component lots in a cGMP cleanroom under supervision. Responsibilities include set-up, operation, deviation investigations, CAPA closures, and aseptic processing with emphasis on documentation and safety.

The role requires basic cell culture knowledge, GMP familiarity, and strong teamwork. Training, cross-functional collaboration, and adherence to GDP/GMP standards are essential for on-time production and quality.

Qualifications

• Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique.
• Knowledge of cGMP/FDA regulated industry.
• Basic mathematical skills.
• General understanding of cGMPs.
• Technical writing capability.
• Proficient in MS Office applications.
• Background to include an understanding of biology, chemistry, medical or clinical practices

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 as needed. Support on time closure of any assigned CAPAs within the designated shift.
• Aseptic technique is required for tube most activities: welding, connections, and transfers, at minimum. Aseptic qualification is required.
• Weighs and measures in-process materials to ensure proper quantities are added/removed.
• Adheres to the production schedule ensuring on-time, internal production logistics.
• Records production data and information in a clear, concise, format according to proper GDPs.
• Perform all tasks in a manner consistent with site safety policies, quality systems, and GMP requirements.
• Works in a team based, cross-functional environment to complete production tasks required by shift schedule.
• Motivated, team consciousness individuals are needed to fulfill job requirements.
• Become a SME and qualified trainer within a designated function of manufacturing.
• Maintain on time completion of training assignments to maintain the necessary technical skills and process knowledge.
• Performs other tasks as assigned: continuous improvement projects, inspection readiness, right first-time initiatives, etc.

Skills

cGMP cell therapy

Aseptic processing

Documentation & GMP records

MS Office

Biology knowledge

Education

High School Diploma

Bachelor's degree or higher

Job description

Bristol Myers Squibb is seeking a Manufacturing Associate to produce blood component lots in a cGMP cleanroom under supervision. Responsibilities include set-up, operation, deviation investigations, CAPA closures, and aseptic processing with emphasis on documentation and safety.

The role requires basic cell culture knowledge, GMP familiarity, and strong teamwork. Training, cross-functional collaboration, and adherence to GDP/GMP standards are essential for on-time production and quality.