CSV Validation Manager – R&D IT Systems

A leading biopharmaceutical company in Paris is seeking a Validation CSV Expert to ensure compliance and quality in R&D IT systems. This role involves defining CSV strategies, managing the full validation lifecycle, and collaborating cross-functionally to maintain audit readiness. The ideal candidate has 6-8 years of experience in CSV within the pharma industry, knowledge of regulatory frameworks, and strong stakeholder management skills. The role is pivotal in balancing innovation and compliance, contributing significantly to patient impact.

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