GxP CSV Specialist – Validation & Compliance Lead
Listed on 2026-10-10
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IT/Tech
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Quality Assurance - QA/QC
Med Pharm Ltd in Guildford is seeking a CSV Specialist to govern and manage validated computerised systems (GxP) across the site, ensuring compliance with EU GMP Annex 11 and MHRA guidance.
You will oversee the validation lifecycle (URS, IQ/OQ/PQ, reports), assess updates, perform risk assessments, and support inspections, collaborating with QA, IT, and operations to maintain data integrity. This on-site role requires 3–5 years CSV experience and a Life Sciences or related degree.
We are looking to fill the GxP CSV Specialist – Validation & Compliance Lead position at Med Pharm Ltd in Guildford, England, United Kingdom.
The GxP CSV Specialist – Validation & Compliance Lead role at Med Pharm Ltd is now open for applications in Guildford, England, United Kingdom.
Join us at Med Pharm Ltd as our next GxP CSV Specialist – Validation & Compliance Lead in Guildford, England, United Kingdom.
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