Cell Therapy Manufacturing Lead - Night Shift

Bristol Myers Squibb

Harvard (MA)

On-site

USD 125,619,000 - 152,211,000

Full time

12 hours ago
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Benefits offered by this job

Flexible Time Off
11 paid company holidays
Stock opportunities / incentive cash

Job summary

Bristol Myers Squibb’s Cell Therapy Manufacturing group seeks a Specialist, Lead Manufacturing Associate Cell Therapy to operate in a GMP environment, with a focus on aseptic processing and equipment setup. The role requires 4+ years in bioprocessing or cell therapy and a relevant bachelor’s degree; night shifts and a rotational schedule are offered in Devens, MA.

You will document batch records, follow SOPs, collaborate with cross-functional teams, and contribute to process improvements while

Qualifications

  • 4+ years of experience in cGMP bioprocessing manufacturing or cell therapy manufacturing.
  • Bachelor's degree in a relevant science or engineering discipline or equivalent work experience.
  • Ability to work night/weekend/holiday shifts and in a cleanroom environment.

Responsibilities

  • Execute operations per SOPs and batch records.
  • Complete documentation per process transfer and batch records.
  • Set up manufacturing areas and equipment; perform commissioning activities.
  • Collaborate with support groups to solve technical problems.
  • Train others on SOPs and Work Instructions.

Skills

cGMP knowledge
Cell therapy manufacturing
Aseptic processing
Cleanroom environment
Shift flexibility

Education

Bachelor's degree in science or engineering

Tools

Automated equipment
Cryopreservation equipment
Biosafety cabinets (ISO 5)

Job description

Bristol Myers Squibb’s Cell Therapy Manufacturing group seeks a Specialist, Lead Manufacturing Associate Cell Therapy to operate in a GMP environment, with a focus on aseptic processing and equipment setup. The role requires 4+ years in bioprocessing or cell therapy and a relevant bachelor’s degree; night shifts and a rotational schedule are offered in Devens, MA.

You will document batch records, follow SOPs, collaborate with cross-functional teams, and contribute to process improvements while

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