**Relocation assistance on offer**
Walker Cole International is searching for a Site Director – Quality Assurance (QA) to join an exciting global biopharmaceutical company based in the South-West of the UK. As a Site Director – Quality Assurance (QA), 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 Director – Quality Assurance (QA) will be to:
- Manage the Site Quality team.
- Ensuring all area activities are cGMP 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 Director – Quality Assurance (QA) 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 cGMP 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
Contact Detail:
Walker Cole International Recruiting Team