GMP Document Control Specialist (DMS) - Veeva Vault Prep
Company: Cpl Life Sciences
Location: Slough
Posted: May 9th, 2026
Cpl Life Sciences is looking for a System Specialist in Slough, United Kingdom, to support their Document Management System (DMS) during a migration to Veeva Vault. This hybrid role involves managing the document lifecycle, acting as a super user for the system, and ensuring compliance with GMP documentation requirements. Candidates should have experience in a GMP pharmaceutical environment and familiarity with DMS tools. Opportunity for high visibility across functions and real impact.
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