QC Microbiology Associate, Cell Therapy

Bristol Myers Squibb EU Policy; Harvard (MA); On-site; USD 51,000 - 62,000; Full time

Benefits offered by this job

Health Coverage

Wellbeing & EAP

401(k) & Insurance

Job summary

Bristol Myers Squibb is seeking an Associate, QC Microbiology, Cell Therapy to join the QC Microbiology team at the Cell Therapy Facility (CTF) in Devens, MA. This role supports testing for in-process, final product, and stability samples, and contributes to environmental and facility monitoring.

The position involves shift coverage Sunday to Wednesday, 6am–4pm onsite, with responsibilities including data verification, document revision, and assistance with deviations and investigations.

Qualifications

• Bachelor's degree preferred in science; associate degree with equivalent experience may be considered.
• 0-2+ years of related microbiological testing or QC experience in a regulated environment preferred.
• Experience with basic laboratory techniques and safety practices.
• Prior microbiological techniques experience is preferred.

Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• Perform environmental/facilities monitoring and microbiological testing.
• May review GMP documentation and perform data verification.
• Support document revision, CAPA and deviation/investigation tasks and continuous improvement efforts.
• May train analysts on general job duties.

Skills

Procedures compliance

Communication

Attention to detail

Team collaboration

Fast-paced environment

Education

Bachelor's degree in science

Associate degree with relevant experience

Tools

GMP Documentation

Laboratory safety practices

Job description

Bristol Myers Squibb is seeking an Associate, QC Microbiology, Cell Therapy to join the QC Microbiology team at the Cell Therapy Facility (CTF) in Devens, MA. This role supports testing for in-process, final product, and stability samples, and contributes to environmental and facility monitoring.

The position involves shift coverage Sunday to Wednesday, 6am–4pm onsite, with responsibilities including data verification, document revision, and assistance with deviations and investigations.