Process Engineer II

Role: Process Engineer II supporting cGMP manufacturing of autologous cell therapies within the MSAT team, focusing on technology transfer, process support, and ongoing commercial production. Responsibilities: lead technical support for GMP runs, conduct investigations using root cause analysis, develop process trending and verification programs, drive continuous improvement projects, coordinate cross-functional tech transfer teams, prepare and review technical documentation, and oversee engineering and process qualification runs. Requirements: Bachelor’s or Master’s in Engineering, Life Sciences, or related field; 3-5 years in biopharma manufacturing, MSAT, or CMC, with experience in cell/gene therapy or biologics preferred; strong knowledge of manufacturing processes, root cause analysis, and project management; excellent communication and leadership skills; familiarity with regulatory standards and statistical tools. HighValue: autologous cell therapies, cGMP environment, tech transfer, process qualification, root cause analysis, process trending, biologics/cell/gene therapy experience. WorkSetup: hybrid Somerville, MA; no travel specified.