Bioprocess Associate
Bristol Myers Squibb
September 03, 2026
Full-time
On-site
Devens, MA
Operations
Role: Bioprocess Associate supporting commercial manufacturing of therapeutic proteins under cGMP conditions. Responsibilities include operating production equipment, adhering to GMPs and SOPs, assisting with process documentation and investigations, maintaining inventory, and supporting a safe work environment. Qualifications: High school diploma required; biotech-related certificate or associates degree preferred. Experience with GMP regulations and clean room environments desirable. Skills: proficiency in computer tools, attention to detail, teamwork, and accountability. High-Value: focus on biologics manufacturing, cGMP compliance, process documentation, and equipment operation. Work setup: on-site at Devens, MA; travel not specified.