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Associate, QC Analytical, Cell Therapy

Bristol Myers Squibb
September 30, 2026
Full-time
On-site
Devens, MA
Operations
Role: QC Analytical Associate supporting testing of in-process, final, and stability samples in cell therapy manufacturing. Responsibilities: perform routine analytical testing, review GMP documentation, assist with deviations, investigations, documentation updates, and continuous improvement. Capable of training analysts and supporting lab tasks. Requirements: Bachelor's in science or equivalent, 0-2+ years in analytical testing or QC, experience with bioanalytical techniques (e.g., cell-based assays, flow cytometry, qPCR), familiarity with GMP environments, attention to detail, effective communication skills. Preferred: cell and molecular biology expertise, experience in regulated biopharma labs. HighValue: cell therapy modalities, in-process/final/stability testing, GMP compliance, laboratory documentation review, continuous improvement, schedule Wed-Sat 6am-4pm, work in Devens, MA.