RC-REGULATORY COMPLIANCE-CSV-Senior

The opportunity We are seeking a highly experienced and detail-oriented Senior CSV Specialist with significant experience in Veeva Vault validation to lead and manage validation activities for GxP-regulated computerized systems. The ideal candidate will ensure compliance with global regulatory standards (FDA, EMA, MHRA) and support cross-functional teams in implementing and maintaining validated systems across the pharmaceutical lifecycle. The role includes implementing and maintaining validated systems across the pharmaceutical lifecycle, including Veeva Vault Quality, Clinical, and RIM applications. This role also involves strategic client engagement, business process transformation, and operational excellence. Your key responsibilities Lead validation efforts for GxP systems using a ris