CAR-T Liso-cel Manufacturing Associate — Night Shift

Bristol Myers Squibb

Summit (NJ)

On-site

USD 38,000 - 46,000

Full time

2 days ago
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Job summary

Bristol Myers Squibb is seeking a Manufacturing Associate for our cell therapy operations in Summit, NJ. The role focuses on producing blood component products under cGMP in a cleanroom, with a shift pattern that includes night hours.

You will participate in equipment setup, perform aseptic tasks, and support quality investigations within a team environment. The position requires a High School Diploma (Bachelor’s or Associate degree preferred) and 0-1 years of cGMP cell therapy experience.

Qualifications

  • High School Diploma required. Bachelor’s or associate degree preferred.
  • 0-1 years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience.

Responsibilities

  • Set-up and operate equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.
  • Support deviation investigations and CAPAs within the shift.
  • Aseptic technique required for tube, welding, connections, and transfers; aseptic qualification required.
  • Weigh and measure in-process materials to ensure proper quantities.
  • Adhere to the production schedule ensuring on-time internal logistics.
  • Record production data clearly and concisely per GDPs and GMP requirements.
  • Work in a cross-functional team to complete production tasks per shift schedule.

Skills

Cell culture basics
Cryopreservation basics
Aseptic processing
C GMP/FDA knowledge
Math skills
Technical writing
MS Office proficiency
Biology/Chemistry background

Education

High school diploma
Bachelor's/Associate degree preferred

Job description

Bristol Myers Squibb is seeking a Manufacturing Associate for our cell therapy operations in Summit, NJ. The role focuses on producing blood component products under cGMP in a cleanroom, with a shift pattern that includes night hours.

You will participate in equipment setup, perform aseptic tasks, and support quality investigations within a team environment. The position requires a High School Diploma (Bachelor’s or Associate degree preferred) and 0-1 years of cGMP cell therapy experience.

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