QC Analytical Specialist – In-Process & Final Product

Bristol-Myers Squibb Co; New Jersey; On-site; USD 72,000 - 88,000; Full time

Benefits offered by this job

Flexible Time Off

Paid holidays

Stock opportunities

Job summary

Bristol Myers Squibb is seeking a Specialist to perform routine testing of in-process, final product, and stability samples to support the Quality Control Analytical department at the Summit, NJ CAR T Manufacturing facility. The role may involve method transfer/validation/verification and documentation revisions, with opportunities to contribute to investigations and continuous improvement.

The position operates on a Wed to Sat PM shift, 1:30pm to 11:30pm, offering exposure to GxP environments

Qualifications

• Bachelor's degree or equivalent; 2+ years of analytical testing or QC experience in a regulated environment.
• Demonstrated experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, aseptic technique).
• We hire for skills and capabilities—if this role excites you but doesn’t perfectly match your resume, apply anyway.

Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• May perform testing for method transfer/validation/verification.
• Train analysts on general job duties and support continuous improvement tasks.

Skills

LIMS

ELN

Problem-solving

Communication

Technical writing

Education

Bachelor's degree or equivalent

Job description

Bristol Myers Squibb is seeking a Specialist to perform routine testing of in-process, final product, and stability samples to support the Quality Control Analytical department at the Summit, NJ CAR T Manufacturing facility. The role may involve method transfer/validation/verification and documentation revisions, with opportunities to contribute to investigations and continuous improvement.

The position operates on a Wed to Sat PM shift, 1:30pm to 11:30pm, offering exposure to GxP environments