QA/ RA Manager

QA/ RA Manager Location: Can be based out of SW London, Guildford, Stoke-on-Trent, Dinnington, Preston or Manchester. We are seeking a QA/ RA Manager to join a growing pharmaceutical manufacturing organisation, taking ownership of regulatory activities while supporting quality operations across the site. This is an excellent opportunity for an experienced Regulatory Affairs professional looking to broaden their influence within a GMP environment, with the longer-term opportunity to apply for an internal Qualified Person (QP) position. Key Responsibilities Lead and coordinate Regulatory Affairs activities across licensed pharmaceutical products. Prepare, review and maintain regulatory submissions including variations, renewals, and new marketing authorisation applications. Act as the primary liaison with regulatory authorities including MHRA. Provide regulatory strategy and guidance to cross-functional teams throughout the product lifecycle. Review technical and regulatory documentation to ensure compliance with applicable GMP and regulatory requirements. Support change controls, deviations, CAPAs and quality investigations from a regulatory perspective. Collaborate with Quality, Manufacturing, Supply Chain and Technical Services teams to ensure continued compliance and supply continuity. Contribute to regulatory intelligence activities and assess the impact of evolving regulations on the business. Required Candidate Profile: Significant Regulatory Affairs experience ..... full job details .....