Process Engineer II

Role: Process Engineer II within Manufacturing Sciences and Technology (MSAT) at Genetix Biotherapeutics, supporting cGMP manufacturing and tech transfer of autologous cell therapies. Responsibilities: serve as technical expert for GMP production at CDMO partners, conduct root cause analyses, develop process trending and verification programs, lead tech transfer teams, prepare technical documentation, analyze process data, support GMP runs, and oversee process qualification. Qualifications: Bachelor’s or Master’s in Engineering, Life Sciences, or related; 3-5 years in biopharma manufacturing or CMC, with experience in cell/gene therapy or biologics preferred; cGMP environment experience essential. Skills: strong problem-solving, project management, communication, statistical analysis, and familiarity with regulatory standards. High-value: focus on autologous cell therapies, cGMP manufacturing, tech transfer, process optimization, and cross-functional collaboration with CDMOs. Work setup: hybrid in Somerville, MA, with an emphasis on proactive problem solving and operational excellence.