Quality Site Manager

1 month ago


Skipton, North Yorkshire, United Kingdom Dechra Pharmaceuticals PLC Full time
Job Description

Dechra Pharmaceuticals PLC is seeking a highly skilled Quality Site Manager to join our team. As a key member of our quality team, you will be responsible for ensuring the implementation and maintenance of quality standards and systems in compliance with UK, EU, and FDA cGMP regulations.

Key Responsibilities:
  • Lead the quality team at our Skipton manufacturing facility, providing strong leadership and guidance to ensure the delivery of high-quality products.
  • Design, develop, and implement a sustainable quality strategy for the site, aligned with the company's 5 strategic pillars.
  • Drive performance improvements across departments, recognizing efficiencies while driving continuous quality improvement.
  • Ensure strategic quality risk management activities are implemented, enabling the identification, mitigation, and escalation of risks that could adversely impact quality compliance.
  • Liaise with regulatory authorities, customers, and suppliers to ensure compliance with current standards and support the implementation of new initiatives.
Requirements:
  • Extensive demonstrated pharmaceutical quality experience, including audit, batch record review, change control, complaint handling, and investigations.
  • Thorough knowledge of pharmaceutical/nutraceutical manufacturing, packaging, testing, and distribution processes, as well as associated global regulatory GMP/GDP requirements.
  • Experience of hosting UK and FDA inspections, client audits, and self-inspections.
  • Technical knowledge to support quality and validation decision-making.
  • Proven track record of working with multi-department projects.

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