Site Quality Director

• Management of the Site Quality team which includes developing and training junior members of the team. 
• Ensure all activities performed on site are cGMP compliant.
• Collaborate and advise across internal business areas, liaising with senior stakeholders across the business.
• 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 Pharmaceutical sectors, or medical devices.
• Extensive experience in a leadership role, with a proven track record of developing, coaching and mentoring junior members of the team. 
• 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 | Quality Management System | QMS | GMP | Good Manufacturing Practice | Manufacturing | Pharmaceutical | Medical Devices | CAPA | Corrective and Preventative Action | Quality | Quality Operations | Deviation | RCA | Root Cause Analysis | Medical Devices | ISO 13485