Evening QC Analytical Specialist — In-Process & Final Product

Bristol Myers Squibb; Denville (NJ); On-site; USD 60,000 - 90,000; Full time

Job summary

Bristol Myers Squibb in Summit, NJ is seeking a Specialist to perform routine testing of in-process, final product, and stability samples in support of the Quality Control Analytical department at the CAR T Manufacturing facility. The role may include method transfer, validation, verification, and GMP documentation review.

Shift: Wed to Sat PM 1:30pm to 11:30pm. Candidates will contribute to data verification, CAPA and deviation investigations, and training of analysts as needed.

Responsibilities

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

Job description

Bristol Myers Squibb in Summit, NJ is seeking a Specialist to perform routine testing of in-process, final product, and stability samples in support of the Quality Control Analytical department at the CAR T Manufacturing facility. The role may include method transfer, validation, verification, and GMP documentation review.

Shift: Wed to Sat PM 1:30pm to 11:30pm. Candidates will contribute to data verification, CAPA and deviation investigations, and training of analysts as needed.