MedPharm Ltd in the United Kingdom seeks a Computer System Validation (CSV) Specialist to govern validation of GxP‑relevant computerised systems on site, ensuring compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, and GAMP5 principles. The role provides technical oversight of electronic systems, manages validation activities, and closes CSV compliance gaps to maintain inspection readiness.
Responsibilities include owning the CSV Master Plan, managing URS/IQ/OQ/PQ, risk assessments,
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GxP CSV Specialist: Validation & Compliance in Guildford employer: MedPharm Ltd
MedPharm is an exceptional employer located in Guildford, offering a dynamic work culture that fosters collaboration and innovation in pharmaceutical research and development. Employees benefit from comprehensive training and growth opportunities, ensuring they can advance their careers while contributing to meaningful projects that impact healthcare. With a commitment to data integrity and compliance, MedPharm provides a supportive environment where analytical scientists can thrive and make a difference.
