Walker Cole International is searching for a Site Quality Director to join an exciting global biopharmaceutical company based in the South-West of the UK.

As a Site Quality Director, you will be responsible for ensuring biopharmaceutical products are released to the highest standard, in line with regulatory body requirements.

Your responsibilities as the Site Quality Director will be to: Manage the Site Quality team.

Ensuring all area activities are c GMP compliant.

Collaborate and advise across internal business areas, liaising with senior stakeholders.

Act as the Quality point of contact for external clients.

Provide oversight of Technical Operations, and support areas including QC, production, and Engineering.

Provide Quality support for audits and regulatory inspections.

Support initiatives to meet or exceed Quality objectives and contribute to continuous improvement planning and execution.

The successful Site Quality Director candidate will have: Significant industry experience in GMP Biopharmaceutical, GMP Pharmaceutical sectors, or medical devices.

Several years in a supervisory role, showing strong leadership.

Technical knowledge of c GMP guidelines, deviation & CAPA management, and audit readiness Quality Assurance | QA | Assurance | Compliance | Operations | Site Quality Director | Head of Quality | Senior Quality Assurance Manager | QA Manager | Supervisor | Team Lead | Quality Management System | QMS | GMP | Good Manufacturing Practice | Manufacturing | Biopharmaceutical | Pharmaceutical | Medical Devices | CAPA | Corrective and Preventative Action | Quality | Quality Operations | Deviation | RCA | Root Cause Analysis | OOS | Out of Specification | OOT | Out of Trend