Lead Quality Officer

Vectura Group


Date: 1 week ago
City: Chippenham, England
Contract type: Full time

At Vectura, we’re driven by innovation and committed to delivering excellence in pharmaceutical development. We’re looking for a Lead Quality Officer who will help shape the future of our Quality function—supporting both the development of life-changing medicines and a culture of continuous improvement.


Why This Role Exists

  • To maintain and improve the Vectura Quality Management System (QMS) in line with GMP and ISO standards
  • To deliver expert Quality Assurance support across projects, especially in the pharmaceutical development, pre-clinical and clinical spaces


What You’ll Be Doing

  • Carrying out a broad range of activities across the QMS including Goods In, environmental monitoring and equipment maintenance
  • Supporting and investigating quality incidents including (but not limited to) deviations, CAPA, change controls, OOS and NCRs.
  • Identifying process improvements and supporting the implementation of changes across the Quality System
  • Generating, reviewing and maintaining all relevant GMP/ISO documentation
  • Conducting detailed reviews of batch manufacturing records and associated test data
  • Leading and performing internal audits, while training and mentoring junior QA staff
  • Working closely with cross-functional project teams and business functions to review and guide quality in documentation
  • Acting as an advocate for quality culture, embedding it across teams
  • Working strategically on onsite archiving, collaborating with our GxP archivist


First 6 Months Snapshot

  • Deep dive into our systems and processes
  • Training and development focused on integration with Pharmaceutical Development principles
  • Support in transitioning and maintaining quality standards in an evolving environment


What You’ll Bring

  • Minimum 2 years in Quality Assurance within pharmaceuticals, ideally with exposure to R&D/Pharmaceutical Development
  • Experience in internal audits, and working knowledge of GMP beyond just the numbers—you know how to apply it
  • Desirable: Exposure to medical devices, combination products, or inhalation product manufacturing/testing
  • Practical mindset, project-savvy, and comfortable mentoring junior colleagues


What We Offer

  • A collaborative, innovation-focused environment
  • A hands-on role with real impact on product quality and patient outcomes
  • Onsite role with limited, ad hoc flexibility for remote working (negotiable based on team needs)


Apply now to join a team where quality is not just a department—it’s a culture.

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