QC Laboratory Supervisor

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.

• 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.

• 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!