Associate, QC Analytical Flow Cytometry, B2 Shift

Role: Support QC testing of in-process, final, and stability samples within a biopharma manufacturing setting, focusing on analytical testing and documentation. Responsibilities: perform routine laboratory tests, review GMP documentation, assist with deviations and investigations, support continuous improvement, and train analysts. Requirements: Bachelor’s degree in science (or Associate’s with relevant experience), 0-2+ years in QC or analytical testing, knowledge of laboratory techniques, and familiarity with GMP practices. Preferred: experience with cell and molecular biology techniques such as flow cytometry and aseptic techniques. HighValue: involvement in biologics manufacturing, supporting QC in regulated environments, with a focus on ensuring product quality during production processes. Work setup: shift-based schedule (Wednesdays-Saturdays, 2PM-12AM) at Devens, MA; travel details not specified.