Site Head Quality

A global leader in the medical device sector is seeking to appoint a Site Head Quality Operations to lead quality strategy and performance at one of its key international manufacturing sites. This appointment follows internal movement and represents an important leadership role within the organisation’s global quality function.

Reporting to the Global Head of Quality, the Director will serve as the senior quality leader for the site, with full accountability for the Quality Management System, regulatory compliance and operational quality performance. The role also carries responsibility as the Quality Management Representative, ensuring the site operates in alignment with global quality standards and applicable regulatory requirements.

As a member of the site leadership team, the Quality Lead will work closely with operations, engineering and global functions to drive quality excellence across manufacturing, strengthen compliance frameworks and embed a culture of accountability, collaboration and continuous improvement.

The successful candidate will lead and develop a high‑performing quality organisation, while influencing senior stakeholders across the global business to ensure consistent delivery of products that meet the highest quality and regulatory standards. xcfaprz

The organisation is seeking an experienced quality leader with a strong background in regulated manufacturing environments. The successful candidate will bring:

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• A degree in Engineering or a related technical discipline
  
• 10+ years of experience in quality leadership roles within the medical device industry
  
• Demonstrated experience leading site‑level quality organisations in regulated manufacturing environments
  
• A track record of driving quality culture transformation and strengthening QMS frameworks
  
• Strong stakeholder engagement and the ability to influence across site and global leadership teams
  

This role offers the opportunity to shape quality strategy at a strategically important site, contribute to the broader global quality agenda, and gain significant visibility within a leading international medical device organisation