I am looking for an experienced Laboratory Supervisor to oversee a small QC analytical team This role will ensure that laboratory operations comply with global regulatory standards, drive continuous improvement, and support audit readiness. Key Responsibilities Lead and manage a QC analytical team of 8/10 direct reports, ensuring all testing activities comply with GMP regulations. Oversee stability testing, ensuring results are accurate and delivered on time. Maintain an inspection-ready QC laboratory and ensure compliance with data integrity guidelines. Manage the laboratory schedule to optimize resources and meet business deadlines. Investigate quality events, deviations, and out-of-specification (OOS) results, ensuring timely resolution. Support the development and validation of analytical methods for routine testing. Ensure all team members are appropriately trained and maintain high documentation standards. Contribute to continuous improvement initiatives to enhance quality and efficiency. What You'll Need 2-3 years experience in a QC leadership role within a GMP-regulated biopharmaceutical or pharmaceutical environment. Stability/QC/analytical R&D/project and program management. Direct supervision of technical staff.(essential) Full understanding of GMP requirements Knowledge and experience of a wide range of techniques, HPLC, UPLC, Electrophoresis, ELISA, spectrophotometry. Why Apply? Contribute to groundbreaking scientific advancements that improve patient health worldwide. Lead a high-performing QC team in a laboratory setting. Career progression opportunities. Be part of a collaborative and forward-thinking organisation. How to Apply: If you're ready for your next challenge, apply now! Skills: Leadership people management GMP Benefits: Benefits