Your new company You'll be joining a global specialty‑pharmaceutical organisation with a strong scientific foundation and a growing UK&I Affiliate team. The company operates across multiple therapeutic areas and is committed to high regulatory and quality standards. The UK team is lean, collaborative, and highly visible to global leadership, giving this role strategic influence across the affiliate. Your new role As the Head of Regulatory Affairs & Quality for the UK & Ireland, you will sit on the UK Senior Management Team and lead all Regulatory Affairs, Quality and local PV activities.You'll provide strategic direction across RA/QA/PV, manage licences (including MIA and WDA(H)), lead MHRA/HPRA interactions, ensure inspection readiness, oversee QMS performance, act as the local PV representative, and drive continuous improvement.You will also lead and develop the RA/QA team, manage consultants, support product launches, oversee market release responsibilities (including RP/RPi/QP‑related duties where required), and act as the key point of contact for both internal global partners and external regulatory authorities. What you'll need to succeed 10+ years of combined Regulatory Affairs and Quality experience within UK/EU pharmaceuticals RP or RPi registration (QP experience is a significant advantage) Strong blend of regulatory lifecycle management and GMP/GDP quality leadership Experience with MHRA inspect...