Process Engineer, MSAT

Role: Mid-level engineer in Manufacturing Sciences and Technology (MSAT), focusing on drug product and process development for ophthalmic hydrogel therapies. Responsibilities: design, execute, and characterize process development studies; develop scalable unit operations; support GMP manufacturing for clinical trials; integrate automation into manual processes; analyze process variables affecting product quality; generate technical documentation; collaborate cross-functionally as an MSAT SME; support late-stage tech transfer and commercial process improvements. Requirements: Bachelor's in Chemical, Biomedical, Mechanical Engineering or related; 4+ years in biopharma process development; experience in cGMP manufacturing; strong scientific, engineering, data analysis, and communication skills; self-motivated team player. Preferred: experience with lab equipment, automated/inspection systems. HighValue: biopharma manufacturing (drug/combination products), GMP/clinical scale, process development, automation, cross-functional collaboration. WorkSetup: full-time onsite Bedford, MA; in a dynamic, fast-paced environment.