Walker Cole International logo

Site Director - Quality Assurance (QA)

Walker Cole International
Department:Manufacturing
Type:ON-SITE
Region:South West England
Location:South West, England, United Kingdom
Experience:Director
Estimated Salary:£80,000 - £120,000
Skills:
QUALITY ASSURANCEGMPBIOPHARMACEUTICALPHARMACEUTICALMEDICAL DEVICESCAPAROOT CAUSE ANALYSISQUALITY MANAGEMENT SYSTEM
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Job Description

Posted on: June 12, 2025

**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

Originally posted on LinkedIn

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