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!
