GxP CSV Specialist: Validate Systems & Data Integrity
Listed on 2026-10-28
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Quality Assurance - QA/QC
Data Analyst -
IT/Tech
Data Analyst
Med Pharm is seeking a CSV Specialist to govern validation and lifecycle management of all GxP computerised systems at site, ensuring ongoing EU GMP Annex 11, MHRA guidance, and data integrity compliance. You will provide technical oversight, manage validation activities, and close CSV gaps to stay inspection-ready.
The role requires hands-on Master Control experience, strong knowledge of GAMP5, and collaboration with QA, IT, and operations to uphold system compliance.
As a GxP CSV Specialist:
Validate Systems & Data Integrity, you will play an important part at Med Pharm in England, United Kingdom.
This is a genuine role to take on the GxP CSV Specialist:
Validate Systems & Data Integrity role at Med Pharm.
We invite applications for the GxP CSV Specialist:
Validate Systems & Data Integrity position located in England, United Kingdom.
The following opportunity is for a GxP CSV Specialist:
Validate Systems & Data Integrity with Med Pharm.
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