CSL is seeking a Validation professional to plan, design, and execute qualification/validation activities in a cGMP environment. You will prepare Validation Master Plans, Project Plans, protocols and Final Reports while coordinating with cross-functional teams.
Responsibilities include maintaining validated state of manufacturing processes, performing risk assessments, and supporting regulatory interactions. Strong collaboration with Manufacturing, MS&T, QE, QA, and Reg Agencies is essential.
#J-18808-LjbffrPharma Validation Engineer — Equity Eligible in kankakee at Unknown Company
This position is listed as full time and onsite.