Quality Specialist I: GMP & Clinical Trial QA (Onsite)
Catalent
Catalent's Kansas City facility is seeking a Quality Specialist I to support clinical trial projects, ensuring GMP compliance and proper documentation. This onsite role emphasizes improving quality systems, maintaining regulatory alignment, and contributing to lifecycle QA activities within a fast-paced environment. The candidate will handle Certificate of Analysis creation under supervision, adhere to GMP standards, and perform multiple QA tasks while supporting continuous improvement #J-18808-Ljbffr Catalent
Vacancy posted 2 days ago
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