Cell Therapy Manufacturing Associate

Biopharma Careers

Harvard (MA)

On-site

USD 34,000 - 41,000

Full time

14 days+

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Benefits offered by this job

Health coverage
Paid time off
On-site facilities

Job summary

Bristol Myers Squibb in Devens, MA is seeking a Manufacturing Associate, Cell Therapy to support routine manufacturing operations under GMP, in a cleanroom environment. You will perform unit operations, document batch records, and contribute to process transfer and equipment setup.

This role requires a high school diploma with 0–2 years in cGMP bioprocessing; a Bachelor's is preferred. You will work day or night shifts, with holidays and weekends on-site, and participate in training to build

Qualifications

  • High school diploma and 0-2 years of experience in cGMP bioprocessing manufacturing or relevant experience.
  • Bachelor's degree in a relevant science or engineering discipline preferred.
  • Willingness to work day or night shifts in a cleanroom environment.

Responsibilities

  • Perform patient process unit operations and support operations per SOPs and batch records.
  • Complete documentation per batch records, transfer and validation protocols.
  • Work in GMP-compliant areas and maintain quality and safety standards.
  • Complete training to ensure necessary technical skills and knowledge.
  • Assist in setting up manufacturing areas and equipment; perform equipment commissioning.
  • Refer to Batch Records and Work Instructions to complete operations.
  • Manage daily unit operations schedule across multiple shifts.

Skills

Cell Therapy Manufacturing
Cleanroom environment
GMP knowledge
Shift flexibility
Documentation & SOPs

Education

High school diploma
Bachelor's degree preferred

Job description

Bristol Myers Squibb in Devens, MA is seeking a Manufacturing Associate, Cell Therapy to support routine manufacturing operations under GMP, in a cleanroom environment. You will perform unit operations, document batch records, and contribute to process transfer and equipment setup.

This role requires a high school diploma with 0–2 years in cGMP bioprocessing; a Bachelor's is preferred. You will work day or night shifts, with holidays and weekends on-site, and participate in training to build

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