QC Analytical Flow Cytometry Associate - 2nd Shift

Bristol-Myers Squibb; Harvard (MA); On-site; USD 50,000 - 62,000; Full time

Job summary

Bristol Myers Squibb is seeking a QC Analytical Flow Cytometry Associate on a B2 shift (Wed-Sat 2PM-12AM) in Devens, MA. Responsibilities include supporting QC testing of samples, documenting processes, and contributing to continuous improvement.

Prior lab experience in cell biology and flow cytometry is preferred. The role emphasizes attention to detail, teamwork, and adherence to GMP practices in a fast-paced environment.

Qualifications

• Bachelor's degree preferred in science.
• Associate’s degree with equivalent education and work experience may be considered.
• 0-2+ years of relevant analytical testing or QC experience in a regulated environment is typical.
• Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.
• Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, aseptic technique) is preferred.

Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• Review GMP documentation and perform data verification.
• Support document revision, project, CAPA and deviation/investigation tasks and continuous improvement efforts.
• May train analysts on general job duties.
• Perform other tasks as assigned.

Skills

QC testing

GMP documentation

data verification

cell biology

laboratory techniques

communication

attention to detail

team collaboration

Education

Bachelor's degree preferred in science

Associate’s degree with equivalent education/experience

Tools

Flow cytometer

Job description

Bristol Myers Squibb is seeking a QC Analytical Flow Cytometry Associate on a B2 shift (Wed-Sat 2PM-12AM) in Devens, MA. Responsibilities include supporting QC testing of samples, documenting processes, and contributing to continuous improvement.

Prior lab experience in cell biology and flow cytometry is preferred. The role emphasizes attention to detail, teamwork, and adherence to GMP practices in a fast-paced environment.