Cell Therapy Manufacturing Associate: Liso-cel CAR-T (Onsite)

Bristol Myers Squibb

Summit (NJ)

On-site

USD 1,543,000 - 1,874,000

Full time

14 days+

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Benefits offered by this job

Health Coverage
401(k) plan
Paid Time Off

Job summary

Bristol Myers Squibb is seeking a Manufacturing Associate, Cell Therapy, to produce human blood components per batch records in a cGMP cleanroom. Work performed under supervision of Manufacturing Management within a team on a production shift schedule.

Attend to deviations and CAPAs as needed and maintain strict aseptic technique. The role requires standing, lifting, and working in restricted cleanroom environments, with training to become SME and trainer within the function.

Qualifications

  • Knowledge 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.

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; aseptic qualification is required.
  • Weighs and measures in-process materials to ensure proper quantities.
  • Adheres to the production schedule ensuring on-time, internal production logistics.
  • Record production data according to GDPs and formats.
  • Follow site safety, quality, and GMP requirements.

Skills

Cell culture knowledge
cGMP/FDA knowledge
Basic math
MS Office
Biology background

Education

High School Diploma
Bachelor's/Associate preferred

Job description

Bristol Myers Squibb is seeking a Manufacturing Associate, Cell Therapy, to produce human blood components per batch records in a cGMP cleanroom. Work performed under supervision of Manufacturing Management within a team on a production shift schedule.

Attend to deviations and CAPAs as needed and maintain strict aseptic technique. The role requires standing, lifting, and working in restricted cleanroom environments, with training to become SME and trainer within the function.

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