CSV Specialist: GxP Systems Lifecycle & Data Integrity
Listed on 2026-09-29
-
IT/Tech
Data Analyst -
Quality Assurance - QA/QC
Data Analyst
Med Pharm seeks a Computer System Validation (CSV) Specialist to govern and manage the lifecycle of GxP computerised systems at the site. You will ensure compliance with EU GMP Annex 11, MHRA guidance, and GAMP5, while providing technical oversight of electronic systems and data integrity.
You will lead validation activities, assess system changes, and close CSV gaps to support inspection readiness. Collaboration with QA, IT, Operations, and vendors is essential.
The CSV Specialist:
GxP Systems Lifecycle & Data Integrity position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the CSV Specialist:
GxP Systems Lifecycle & Data Integrity role at Med Pharm, based in England, United Kingdom.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).