Bioprocess Associate

Role: Bioprocess Associate responsible for executing commercial manufacturing processes of therapeutic proteins under cGMP standards. Responsibilities include operating and maintaining production equipment, adhering to GMP and SOPs, revising process documents, supporting investigations, and managing materials inventory. The role emphasizes process automation, safety, and routine manufacturing tasks within a regulated environment. Requirements: high school diploma; preferred associate degree or biotech certification; GMP or clean room experience desirable; proficiency with computer tools; prior experience in a regulated biotech or pharmaceutical setting preferred. High-Value: manufacturing biologics, therapeutic proteins, cGMP compliance, supporting process documentation and investigations. Work setup: evening shift (M-F, 2pm-10pm), Devens, MA.