The Role We’re looking for an experienced Quality leader to take charge of a well-established UK pharmaceutical manufacturing site, specialising in unlicensed medicines (Specials). You’ll be responsible for safeguarding compliance, driving operational excellence, and embedding a culture of patient safety and continuous improvement. What You’ll Do * Lead and evolve the site’s Quality Management System (QMS), ensuring best-in-class GMP/GDP compliance. * Be the driving force behind MHRA inspection readiness and regulatory excellence. * Partner with the Responsible Person (RP) to connect manufacturing, quality, and distribution seamlessly. * Champion a culture of continuous improvement, empowering your team to deliver Right First Time, every time. * Influence senior leadership and the board with data-driven insights, KPIs, and risk strategies. * Build and mentor a high-performing QA/QC function, with clear succession planning and development pathways. About You * Degree in Pharmacy, Pharmaceutical Sciences, or related discipline (MSc/PhD welcome). * Eligible to be named on a Manufacturer’s “Specials” Licence; QP status would be a real advantage. * At least 5 years’ experience in pharma manufacturing, with strong exposure to Specials. * Proven leader with the confidence to engage regulators, inspire teams, and influence stakeholders at every level. * Analytical, adaptable, and committed to keeping patients at the heart of every decision. Why This Role? * Impact: Play a central role in safeguarding patients and raising standards in a critical area of UK pharma. * Leadership: Shape site strategy and lead a capable team with the autonomy to make real changes. * Growth: Develop your own career while building the next generation of quality leaders. * Visibility: Work directly with the board, regulators, and cross-functional teams in a high-profile role