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Senior Bioprocess Associate

Bristol Myers Squibb
September 09, 2026
Full-time
On-site
Devens, MA
Operations
Role: Senior Bioprocess Associate supporting commercial biotech manufacturing of therapeutic proteins using cGMP standards. Responsibilities: execute routine manufacturing tasks, operate primary equipment (bioreactors, chromatography skids), maintain materials inventory, revise process documents, assist with investigations, and ensure compliance with safety and regulatory requirements. Requirements: high school diploma; 2+ years of process operations experience in GMP-regulated biotech manufacturing; knowledge of GMP/SOP; proficiency with automation systems (e.g., Delta V, Syncade) and business tools (e.g., SAP); strong attention to detail and teamwork skills. Preferred: background in science or engineering, familiarity with biotech manufacturing processes. HighValue: biologics, therapeutic proteins, commercial manufacturing, cGMP, process automation, process documentation, inventory management. WorkSetup: night shift (M-TH, 9:30 pm–7:30 am); Devens, MA.