The Supervisor, Manufacturing oversees GMP clinical drug substance production, managing technicians and ensuring successful manufacturing campaigns.
Key responsibilities include day-to-day people management—setting expectations, training, performance reviews, and fostering a safety-focused team culture.
They troubleshoot complex process issues, monitor operations for smooth execution, and proactively address scheduling and resource needs.
Ensuring compliance with GMP standards, reviewing batch records, and collaborating with quality teams are essential.
Qualifications include a science or engineering degree, 5+ years in biotech/pharma GMP manufacturing, and experience in people management.
Proficiency in GMP regulations, process automation, SAP, and electronic systems is required. The role involves critical thinking, decision-making, continuous improvement, and working shift hours in a dynamic environment.