QC Flow Cytometry Analyst – Entry Level

Bristol-Myers Squibb; United States; On-site; USD 51,000 - 62,000; Full time

Benefits offered by this job

Wellbeing support

Retirement and financial protection—p5

Insurance offerings

Job summary

Bristol Myers Squibb is seeking a QC support analyst to assist in testing in-process, final product, and stability samples. You will contribute to documentation, deviations, investigations, and continuous improvement, with a Wednesday-Saturday 2 PM–12 AM shift.

Ideal candidates have 0–1+ years in analytical QC in regulated environments, coupled with basic lab techniques and strong attention to detail. Join a team focused on delivering high-quality medicines.

Qualifications

• Bachelor's degree in science preferred; Associate's degree with equivalent education/work experience may be considered.
• 0-1+ years of relevant analytical testing or QC experience in a regulated environment.
• Experience with basic laboratory techniques and safety practices.
• Prior experience in cell/molecular biology techniques (cell-based assays, flow cytometry, aseptic technique) preferred.
• Ability to follow procedures accurately and communicate effectively with peers and management.

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.
• May train analysts on general job duties.
• Perform other tasks as assigned.

Skills

Attention to detail

Communication skills

Teamwork

Adaptability

Education

Bachelor's degree in science

Associate's degree with equivalent experience

Tools

Flow cytometry

Cell-based assays

Job description

Bristol Myers Squibb is seeking a QC support analyst to assist in testing in-process, final product, and stability samples. You will contribute to documentation, deviations, investigations, and continuous improvement, with a Wednesday-Saturday 2 PM–12 AM shift.

Ideal candidates have 0–1+ years in analytical QC in regulated environments, coupled with basic lab techniques and strong attention to detail. Join a team focused on delivering high-quality medicines.