MedPharm 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.
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CSV Specialist: GxP Systems Lifecycle & Data Integrity employer: MedPharm
As a Computer System Validation Specialist at our site, you will join a dynamic team dedicated to ensuring compliance and data integrity in a supportive work environment. We prioritise employee growth through continuous training and development opportunities, fostering a culture of collaboration and innovation. Located in a vibrant area, we offer unique advantages such as flexible working arrangements and a commitment to work-life balance, making us an excellent employer for those seeking meaningful and rewarding careers in the pharmaceutical industry.
