ARM International is seeking a Computer System Validation (CSV) Consultant to join its growing life sciences consultancy team. The role focuses on leading CSV activities across pharma, biotech, and medical device projects in a collaborative, international environment. You will author and review validation plans, URS, risk assessments, IQ/OQ/PQ protocols, and summary reports, while ensuring compliance with GMP, Gx P, Annex 11, and 21 CFR Part 11 across multiple client engagements. #J-18808-Ljbffr
📌 Senior csv consultant – life sciences validation expert (Madrid)
🏢 ARM International
📍 Madrid
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