QC Analyst, Flow Cytometry & In-Process Testing

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

Job summary

Bristol Myers Squibb is seeking a QC Analyst to support in-process, final product, and stability testing at our Devens, MA site. The role emphasizes documentation, data verification, and continuous improvement in a fast-paced environment.

Responsibilities include training analysts, reviewing GMP records, and assisting with deviations and investigations while maintaining strict quality standards and regulatory compliance.

Qualifications

• Bachelor's degree in science preferred; relevant experience considered.
• 0-2+ years of analytical testing or QC experience in a regulated environment.
• Basic lab techniques and safety practices.

Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• May review GMP documentation and perform data verification.
• Support document revision, CAPA and deviation/investigation tasks.

Skills

Laboratory techniques

Cell biology

Communication

Attention to detail

Teamwork

Education

Bachelor's degree in science

Associate’s degree with equivalent experience

Tools

Flow cytometer

Laboratory instrumentation

Job description

Bristol Myers Squibb is seeking a QC Analyst to support in-process, final product, and stability testing at our Devens, MA site. The role emphasizes documentation, data verification, and continuous improvement in a fast-paced environment.

Responsibilities include training analysts, reviewing GMP records, and assisting with deviations and investigations while maintaining strict quality standards and regulatory compliance.