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