GMP Validation Specialist: IQ/OQ/PQ for Syringe Machines
Katalyst CRO
A leading pharmaceutical company is seeking a Validation Specialist to support validation activities for Syringe Assembly Machines in a GMP-compliant environment. The ideal candidate will have at least 2 years of experience and a solid understanding of validation lifecycle documentation. Key responsibilities include performing validation activities, developing validation protocols, and collaborating with cross-functional teams. This is a contract position offering a competitive hourly rate based on experience. #J-18808-Ljbffr Katalyst CRO
Vacancy posted 2 days ago
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