Pharmaceutical Development and Clinical Manufacturing Supervisor

This role provides frontline leadership to supervise daily Pharmaceutical Development and Clinical Manufacturing operations, ensuring production activities are planned, staffed, and executed safely and in compliance with cGMP and regulatory standards. The position coordinates closely with cross-functional teams to support project timelines, production readiness, and reliable client delivery for oral solid dose development and clinical trial material manufacture. It involves direct supervision of production team members, ensuring accurate documentation, equipment readiness, and adherence to safety and quality expectations.