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Quality Systems Manager (and Data Lead)

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GSK

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Location:
United Kingdom , Barnard Castle

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Category:

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Contract Type:
Not provided

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Salary:

Not provided

Job Description:

We are looking for a senior quality management professional to lead a high-performing team of quality specialists at our Barnard Castle manufacturing site. Reporting into the site’s Quality Director, The Quality Systems and Data Lead is responsible for the effective management, oversight, and continuous improvement of the Barnard Castle site’s Quality Management Systems (QMS) and associated data processes. This role is a senior position within the site’s quality management team. It ensures compliance with regulatory requirements, drives data integrity, and fosters a culture of quality excellence across the Barnard Castle site. Working cross-functionally you will coordinate efforts to enhance quality systems, as well as integrate digital innovation initiatives and data governance frameworks.

Job Responsibility:

  • Manage and oversee the site’s Quality Management System (QMS) processes to ensure compliance with GMP standards
  • Provide oversight and expert guidance on the development, management, and tracking of CAPAs and deviations
  • Act as primary liaison for quality audits
  • Manage governance and implementation of robust Data Integrity (DI) practices
  • Drive innovation in quality systems via digital tools and technologies
  • Develop and maintain quality documentation systems
  • Ensure training compliance across the site by designing, delivering, and monitoring effective quality training programs
  • Manage and develop a high-performing team of specialists
  • Foster collaboration across departments, functions and processes
  • Leverage AI tools and technologies to enhance the performance and efficiency of quality systems and processes

Requirements:

  • Degree in relevant Scientific, Technical or Engineering discipline or equivalent experience (ideally gained working in a manufacturing facility from a highly-regulated industry)
  • Management experience
  • Knowledge of current Good Manufacturing Practice (cGMP) requirements
  • Knowledge and application of Quality Management Systems (QMS)
  • Knowledge of internal and external audit processes (eg
  • inspection readiness)
  • Strong people management skills
  • Proven ability to influence people to achieve objectives and drive performance
  • Strong experience of working in regulatory or quality functions and/or manufacturing at a complex highly-regulated manufacturing site

Additional Information:

Job Posted:
January 31, 2026

Expiration:
February 15, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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