Quality Assurance Documentation Lead

1 day ago


Oxford, Oxfordshire, United Kingdom Oxford Biomedica Full time

Oxford Biomedica seeks a highly skilled Document Controller to join its Quality Assurance team. This role involves providing critical GxP documentation support for manufacturing, research, and validation activities while ensuring the effective maintenance of document control systems.

The Quality Assurance team at Oxford Biomedica plays a crucial role in maintaining the company's quality processes and systems in accordance with GMP guidelines. They oversee internal and external audits, quality compliance, and control.

  • Maintain accurate and up-to-date documentation within electronic document management systems and paper-based filing systems.
  • Provide administrative support for electronic document management systems and troubleshoot document creation issues.
  • Prepare and manage documentation for offsite archives and retrieve documents as needed.

Key Responsibilities:

  • Ensure compliance with GMP guidelines and regulations.
  • Maintain accurate records and documentation.
  • Collaborate with the Quality Assurance team to ensure effective document control systems.

Salary and Benefits:

This role offers a competitive salary range of £48,000 - £58,000 per annum, depending on experience, plus benefits including access to state-of-the-art facilities.

About Us:

Oxford Biomedica is a leading viral vector CDMO that partners with global pharmaceutical and biotechnology companies to develop and manufacture life-saving treatments. Our team has extensive experience in viral vector development and manufacturing.

What We Offer:

  • Competitive salary and benefits package.
  • Opportunities for professional growth and development.


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