Validation Engineer - Pharma cGMP & Sterile Systems
Yoh, A Day & Zimmermann Company
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-Ljbffr Yoh, A Day & Zimmermann Company
Vacancy posted 10 hours ago
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