MedPharm 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 MasterControl experience, strong knowledge of GAMP5, and collaboration with QA, IT, and operations to uphold system compliance.
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GxP CSV Specialist: Validate Systems & 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.
