Cell Therapy QC Analyst – In/Final Product

Bristol Myers Squibb; Summit (NJ); On-site; USD 48,000 - 58,000; Full time

Job summary

Bristol Myers Squibb in Summit, NJ is hiring a QC analyst to support in-process, final product and stability testing. You will review data, assist with method transfer and deviations, and contribute to continuous improvement in a fast-paced team.

The role requires a Bachelor's in science and 2+ years of analytical QC experience in a regulated environment, with familiarity in LIMS/ELN. Shift is Wednesday through Saturday, 1:30pm–11:30pm, with comprehensive benefits and growth opportunities.

Qualifications

• Bachelor's degree in science or equivalent.
• 2+ years of analytical testing or QC experience in a regulated environment.
• Experience with cell/molecular biology techniques (e.g., qPCR, ELISA, flow cytometry).

Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• Perform testing for method transfer/validation/verification.
• Perform data verification, data review and review of GMP documentation for general methods.
• May perform document revision, CAPA and deviation/investigation tasks and continuous improvement efforts.
• Train analysts on general job duties.
• Perform other tasks as assigned.

Skills

QC testing

Data review

cGMP knowledge

Communication

Documentation

Team collaboration

Education

Bachelor's degree in science

Tools

LIMS

ELN

Job description

Bristol Myers Squibb in Summit, NJ is hiring a QC analyst to support in-process, final product and stability testing. You will review data, assist with method transfer and deviations, and contribute to continuous improvement in a fast-paced team.

The role requires a Bachelor's in science and 2+ years of analytical QC experience in a regulated environment, with familiarity in LIMS/ELN. Shift is Wednesday through Saturday, 1:30pm–11:30pm, with comprehensive benefits and growth opportunities.