CSV Specialist: Data Integrity & Validation Lead

MedPharm is seeking a CSV Specialist to govern and validate GxP computerised systems at our site, ensuring compliance with EU GMP Annex 11, MHRA guidance, and GAMP5 principles. You will oversee the validation lifecycle, assess updates, and close CSV gaps to maintain inspection readiness and data integrity.

You will work with QA, IT and operations to define validation plans, support regulatory inspections, and develop templates aligned with best practices.

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