Downstream Biomanufacturing Sciences Specialist

A Downstream Biomanufacturing Sciences Specialist in Clinical Manufacturing ensures manufacturing area efficiency and product compliance with GMP, Health, Safety, and Environmental regulations by optimizing daily activities. The role involves autonomously supporting the full lifecycle of clinical campaigns, including preparation, execution, and release of technical and GMP batches for phases I, II, and III. Additionally, the specialist manages process transfers, data interpretation, deviation control, and acts as a project lead for downstream field operations within the Bio Drug Substance team.