Senior CSV Lead for GxP Validation (Pharma, Hybrid)

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Description

Oxford Global Resources Life Sciences is seeking a CSV specialist with 2 years of experience to join our client in the Barcelona area on a hybrid basis.

You will drive validation activities for GxP-regulated systems within the IT organization.

You will author validation plans, IQ/OQ/PQ protocols and traceability matrices, execute testing, manage change controls, and support regulatory inspections.

This is a long-term opportunity with potential internalization within the client.

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