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, GxP, Annex 11, and 21 CFR Part 11 across multiple client engagements.
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📌 Senior CSV Consultant – Life Sciences Validation Expert (Cataluña)
🏢 ARM International
📍 Cataluña
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