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 7 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
- Level 8 degree in Pharmaceutical Science, , Biology, Chemistry, or other scientific discipline
- 2 years experience in a QC leadership role within a GMP-regulated biopharmaceutical or pharmaceutical environment.
- QC/analytical R&D/project management.
- Direct supervision of technical staff. (essential)
- Full understanding of GMP requirements
- Knowledge and experience of a wide range of techniques in bioassays including polymerase chain reaction (qPCR and RT-PCR) and enzyme linked immunosorbent assays (ELISA) would be benefical
How to Apply: If you’re ready for your next challenge, apply now!
