Yoh is seeking a Validation Engineer for a pharmaceutical manufacturing client in Noblesville, IN. The role focuses on hands-on validation activities for CIP systems, sterile processes, and associated utilities within a GMP environment.
Responsibilities include leading validation lifecycle activities, coordinating cross-functionally, and producing validation reports. Familiarity with temperature mapping tools and regulatory requirements is required. Competitive benefits apply.
#J-18808-LjbffrValidation Engineer – Pharma cGMP & Sterile Systems in noblesville at Unknown Company
This position is listed as full time and onsite.