CQV Lead, OSD GMP Validation & Digital Compliance
Katalyst CRO
Katalyst CRO in the Town of Florida, New York, is seeking a CQV Lead with strong engineering fundamentals and hands-on experience in commissioning, qualification, and validation in a GMP-regulated Oral Solid Dose (OSD) environment. This role includes leading CQV activities for manufacturing systems, ensuring compliance with regulations, and collaborating with cross-functional teams to deliver validated systems. The ideal candidate holds a Master's or PhD in Engineering with at least 3 years of relevant experience. #J-18808-Ljbffr Katalyst CRO
- ...Summary We are seeking a CQV Lead (OSD Manufacturing) with strong... ...commissioning, qualification, and validation within a GMP‑regulated Oral Solid Dose... ...expertise with a modern, digital‑first approach to... ...validation deliverables Ensure compliance with data integrity...Digital
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