Cell Therapy Manufacturing Associate – GMP, Onsite

Bristol-Myers Squibb Co; Summit (NJ); On-site; USD 38,000 - 46,000; Full time

Job summary

Bristol Myers Squibb in Summit, NJ, is hiring a Manufacturing Associate to support Liso-cel CAR-T production in a cGMP cleanroom. You will operate equipment, ensure production quality, and contribute to on-time delivery of cell therapy components under supervision of Manufacturing Management.

Responsibilities include set-up and operation of equipment, assisting with deviation investigations, aseptic processing, data recording, and adherence to GDP and GMP.

Qualifications

• High School Diploma required; Bachelor's or Associate degree preferred.
• Understanding of biology, chemistry, medical or clinical practices is advantageous.
• Experience with cell therapy manufacturing is a plus.

Responsibilities

• Set-up and operation of equipment to support production of blood components through cell culture, harvest, and cryopreservation.
• Support deviation investigations and CAPA closures during shift.
• Aseptic technique required for all tube-related activities and aseptic qualification.
• Weighs and measures in-process materials to ensure proper quantities.
• Adheres to the production schedule ensuring on-time logistics.
• Record production data accurately according to GDPs.
• Operate within GMP and safety policies; maintain cleanroom discipline.
• Work in a cross-functional team to complete shift tasks.
• Demonstrate motivation and team orientation for the role.
• Become SME and trainer within designated manufacturing function.

Skills

Basic understanding of cell culture

GMP/FDA knowledge

Mathematical skills

CGMP understanding

Technical writing

MS Office

Biology/chemistry background

Education

High School Diploma

Bachelor's or Associate degree

Tools

MS Office

Job description

Bristol Myers Squibb in Summit, NJ, is hiring a Manufacturing Associate to support Liso-cel CAR-T production in a cGMP cleanroom. You will operate equipment, ensure production quality, and contribute to on-time delivery of cell therapy components under supervision of Manufacturing Management.

Responsibilities include set-up and operation of equipment, assisting with deviation investigations, aseptic processing, data recording, and adherence to GDP and GMP.