MedPharm Ltd in the United Kingdom seeks a Computer System Validation (CSV) Specialist to govern validation of GxP‑relevant computerised systems on site, ensuring compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, and GAMP5 principles. The role provides technical oversight of electronic systems, manages validation activities, and closes CSV compliance gaps to maintain inspection readiness.
Responsibilities include owning the CSV Master Plan, managing URS/IQ/OQ/PQ, risk assessments,
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This role is for the GxP CSV Specialist: Validation & Compliance role at MedPharm Ltd.
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