Quality Manager

  • {{workoutLocation({display_location: '', country: 'United Kingdom', town: 'Oxfordshire'})}}
  • Undisclosed
  • Permanent
  • Oliver Page
  • 02392 314792
  • Email about this job

As the Quality Assurance Manager, you will responsible for supporting the CMC group consisting of manufacturing science and technology, analytical development and clinical supply teams. Other key responsibilities within the position will be to (Not limited to):

* Ensuring compliance with GMP and other regulatory requirements; be the Quality point of contact for CMC external parties; manage the review and timely closure of manufacturing and/or release and stability testing deviations or change controls.

* Responsible for management of the CMC part of the annual External/Supplier audit programme

* To provide guidance for higher level decisions required for change management and deviation investigations, as required.

The preferred candidate for the role will have extensive experience in GB and EU GMP regulated environments and would have acted as quality manager in a pharmaceutical or Biotechnology organisation with Biologics manufacturing experience. The ideal candidate will also have good understating of IMP manufacturing and extensive expertise of EU, MHRA and FDA requirements

If you are interested in this opportunity, please send your up-to-date CV to Oliver@BlackfieldAssociates.com or call Oliver on 02392 314 792.

STR Limited is acting as an Employment Agency in relation to this vacancy.



Health Economics & Outcomes Research


Market Access, Pricing & Reimbursement

Medical Affairs

Quality Assurance




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