MedPharm is seeking a CSV Specialist to govern and validate GxP computerised systems at our site, ensuring compliance with EU GMP Annex 11, MHRA guidance, and GAMP5 principles. You will oversee the validation lifecycle, assess updates, and close CSV gaps to maintain inspection readiness and data integrity.
You will work with QA, IT and operations to define validation plans, support regulatory inspections, and develop templates aligned with best practices.
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CSV Specialist: Data Integrity & Validation Lead 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.
