Process Supervisor

Process Supervisor at Pfizer’s Ringaskiddy Clinical Manufacturing Facility (RCMF) overseeing end-to-end manufacturing programmes for late-stage clinical API production. Lead transfer of processes and technologies from R&D labs and external partners into the manufacturing facility; shape safe, efficient, and compliant manufacturing campaigns; develop procedures, training materials, and manufacturing records to support cGMP manufacturing; provide technical leadership in troubleshooting during start-up and operations; contribute to clinical process development and the delivery of clinical supply; support progression toward commercial launch and transfer of processes to commercial manufacturing; collaborate with Quality Operations, Analytical R&D, Logistics, Global Materials Management, Engineering and other cross-functional teams; drive continuous improvement in safety, quality, compliance, delivery and performance; monitor process performance through data collection and technical review; coach and develop the team; maintain inspection readiness. Requires a BSc in a related discipline and 3-5 years in commercial or clinical small molecule API manufacturing or technical transfer; strong technical, problem-solving and communication skills; ability to work in a high-performance, start-up environment.