Site Quality Director – North Yorkshire

Pharmaceutical / GMP Manufacturing

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A leading GMP manufacturer in North Yorkshire is seeking to appoint a Site Quality Director. This is a senior leadership role with responsibility for site-wide quality operations, regulatory compliance, and strategic development of quality systems within a regulated pharmaceutical manufacturing environment.

The Role

Reporting at site leadership level, you will oversee Quality Control, Quality Assurance and Qualified Person activities, ensuring compliance with UK, EU and FDA cGMP requirements. You will lead the development and execution of the site quality strategy, embedding robust systems and driving continuous improvement across all quality functions.

Key responsibilities include: