As a Process Engineer III, you'll lead downstream processing projects, collaborate with teams, ensure compliance with regulations, and drive continuous improvement in biopharmaceutical manufacturing.

Lead global MSAT technology transfer and process validation for late-stage and commercial biologics. Drive site-to-site transfers, develop global templates/protocols (PPQ, PQ, batch records), perform gap/risk analyses and mitigation, analyze process data and annual reviews, support regulatory CMC documentation and inspections, and mentor junior engineers.