Senior CSV Lead for GxP Validation (Pharma, Hybrid)

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. J-18808-Ljbffr