Validation Pharmacists >
Description.
Oversee and execute validation activities for pharmaceutical production, aseptic preparation, and quality systems within MHRA-regulated, GMP-compliant environments. Ensure equipment, processes, and documentation meet regulatory and company standards to support safe, consistent manufacture of medicinal products.Key Requirements.
Experience.
GPhC-registered Pharmacist with a minimum of 2 years’ validation or quality systems experience in a GMP-regulated pharmaceutical, aseptic, or hospital manufacturing environment.
Skilled in process validation, equipment qualification and requalification, and protocol development (IQ/OQ/PQ).
Experience managing deviations, change controls, and CAPA actions linked to validation or quality issues.
Confident working with multidisciplinary teams including QA, QC, engineering, production, and regulatory affairs.
Qualifications.
MPharm degree (or recognised equivalent) with full GPhC registration.
Postgraduate qualification in Validation, Quality Systems, Pharmaceutical Technology, or a related GMP discipline preferred.
Ongoing CPD in GMP, quality management, validation methodology, or regulatory compliance.
Compliance and Vetting.
Enhanced DBS
Full identity and right-to-work verification.
Two recent professional references.
Up-to-date mandatory training appropriate to the manufacturing or technical setting.
Immunisation compliance where roles involve clean-room, aseptic units, or hospital manufacturing.
Full GPhC registration and fitness-to-practise check.
Verification of qualifications, validation training, and employment history.