GMP Validation Leader: Qualification & CSV Expert
Katalyst CRO
Katalyst CRO is seeking an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. You will plan, execute, review, and approve validation documentation for equipment, facilities, processes, and computerized systems while ensuring compliance with FDA, EMA, and cGMP regulations. Responsibilities include leading DQ/IQ/OQ/PQ lifecycle, authoring validation documents, managing deviations and CAPAs, and collaborating with Quality #J-18808-Ljbffr Katalyst CRO
Vacancy posted 2 days ago
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