Staftonic LLC is seeking a CQV Lead to drive commissioning, qualification, and validation activities in a GMP manufacturing environment. The role involves hands-on work with packaging processes, protocol execution, and real-time troubleshooting on the floor.
You will develop IQ/OQ/PQ documents, apply Minitab for process characterization, and perform advanced statistical analyses. Strong writing and cross-functional collaboration are essential for successful commercialisation.
#J-18808-LjbffrSenior CQV Engineer - GMP Validation & Process Optimization in ky at Unknown Company
This position is listed as full time and onsite.