We are looking for a permanent QP to support the manufacture and release of radiopharmaceuticals at a UK production facility based in Nottingham. Will also be happy to look at someone who has extensive sterile batch release expertise.
About the OrganisationThepany is a major international provider of advanced healthcare technologies, operating globally.
The RoleAs a QP, you will take a central role in ensuringpliant, timely product release and maintaining the highest standards of quality across the manufacturing process. Responsibilities include: Product Certification &pliance
1. Certify and release batches in alignment with UK and EU GMP – 4+ batches per day.
2. Ensure all documentation, testing, and manufacturing records meet regulatory expectations.
Quality Assurance
3. Oversee QC testing, deviations, CAPAs, and related manufacturing and supply chain documentation.
4. Support continuous improvement initiatives within the quality function.
Quality Management System (QMS)
5. Lead the site QMS and collaborate with wider UK/European quality teams to ensure harmonised,pliant practices.
6. Input into audits, inspections, and qualityernance activities.
Your Background
7. Degree in a Life Sciences discipline.
8. Eligible to act as a QP in the UK under the Human Medicines Regulations for Sterile Manufacturing or Radiopharmaceuticals.
9. Strongmunication skills and a solutions‑oriented approach.
10. In‑depth knowledge of GMP and experience across the pharmaceutical product lifecycle.
Benefits
11. Additional Bonus allowance
12. Flexible benefits package + Great Pension Contribution
13. 26 days’ annual leave.
14. Share scheme options.
15. Paid volunteering days.
Contact details: If you are interested and have radiopharmaceuticals or sterile manufacturing batch release expertise and are open to working in Nottingham full time, please get in touch with J or +443330106057 #4770276 - Julia Bowden