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Site Quality Director

WALKER COLE INTERNATIONAL LTD
Posted 12 hours ago, valid for 17 days
Location

Dulverton, Somerset TA22 9HL, England

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • Walker Cole International is seeking a Site Quality Director for a global biopharmaceutical company in South-West UK.
  • The role involves managing the Site Quality team and ensuring compliance with cGMP regulations for biopharmaceutical products.
  • Candidates should have significant industry experience in GMP biopharmaceuticals or medical devices, along with several years in a supervisory role.
  • Technical knowledge of cGMP guidelines and audit readiness is essential for this position.
  • The salary for the Site Quality Director role is competitive and commensurate with experience, typically requiring over 5 years in a relevant field.

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 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 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 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

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.