CAR-T Cell Therapy Manufacturing Associate – Overnight Shift

Bristol Myers Squibb

Summit (NJ)

On-site

USD 39,000 - 47,000

Full time

2 days ago
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Job summary

Bristol Myers Squibb is seeking a Manufacturing Associate in Summit, NJ to support cell therapy production in a cGMP cleanroom. You will operate equipment, follow batch records, and work under supervision to meet production schedules.

You will participate in deviation investigations, CAPAs, and continuous improvement while maintaining aseptic techniques and proper documentation. Onsite shift, safety, and quality are priorities.

Qualifications

  • Minimum high school diploma; an associate or bachelor's degree is preferred.
  • 0–1 year of cGMP cell therapy manufacturing or related experience.
  • Basic understanding of cell culture, cryopreservation, and aseptic processing.
  • Knowledge of cGMP/FDA regulated industry.
  • Proficient with MS Office applications.

Responsibilities

  • Set up and operate equipment to support production of blood component lots.
  • Support deviation investigations and CAPA closure within the shift.
  • Aseptic technique required for all activities; aseptic qualification required.
  • Record production data clearly and concisely per GDP standards.
  • Work in a cross-functional team to meet shift production goals.
  • Participate in training and become SME trainer in a designated function.
  • Adhere to safety, quality, and GMP requirements.

Skills

Cell culture
Cryopreservation
Aseptic processing
cGMP
FDA compliance
Math skills
MS Office
Biology knowledge

Education

High school diploma
Associate degree preferred
Bachelor's degree preferred

Job description

Bristol Myers Squibb is seeking a Manufacturing Associate in Summit, NJ to support cell therapy production in a cGMP cleanroom. You will operate equipment, follow batch records, and work under supervision to meet production schedules.

You will participate in deviation investigations, CAPAs, and continuous improvement while maintaining aseptic techniques and proper documentation. Onsite shift, safety, and quality are priorities.

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