Aseptic Fill-Finish Validation Lead

A leading biopharmaceutical company is seeking a Validation Engineer to support aseptic process validation for sterile injectable products. The role focuses on ensuring compliance with FDA and regulatory requirements, particularly in vial filling and fill-finish operations. Ideal candidates will have 4–8 years of related experience, a solid understanding of cGMP regulations, and excellent technical writing skills. The position requires close collaboration with Manufacturing and Quality Assurance teams in a compliance-focused environment.
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