QP

We are seeking an experienced Qualified Person (QP) with IMP experience to join a leading pharmaceutical company in Greater London. This is a fantastic opportunity to play a key role in ensuring the highest standards of compliance and product quality within a dynamic and growing organisation. Key Responsibilities: * Act as a QP for the certification and release of IMPs in compliance with EU GMP regulations. * Ensure adherence to quality standards, regulatory requirements, and clinical trial protocols. * Work closely with cross-functional teams, including Regulatory Affairs, Manufacturing, and Quality Assurance. Requirements: * QP status eligible under Directive 2001/83/EC. * Strong IMP experience within a GMP environment. * Excellent knowledge of EU and UK pharmaceutical regulations. 📍 Location: Greater London Area (4 days on-site, 1 day from home) 💰 Competitive salary + benefits Interested? Apply now