Supplier Quality Manager

Quality Manager, focused on Supplier Audits (m / w / d)


Based in Frankfurt


My client is a global, market leading medical device manufacturer. The company are very well known, highly regarded, and offer drug device combination products up to Class III. The position is focused on supplier auditing and management, and is part of a global RA/QM division.


Your Responsibilities:

  • Drafting service agreements with suppliers and service providers (eg contract manucaturers, warehouses or laboratories)
  • Supplier audits in consideration of those service agreements, providing support and guidance
  • Internal audits across multiple departments on a global scale
  • SOPs & Validation
  • Maintenance of the QMS (ISO 13485) and working closely with the RA department on the new regulations (MDD/MDR transition)
  • A close partnership with other departments


Experience Required:

  • Degree educated in scientific studies or engineering
  • 2-4 years of experience in Quality Management at a medical device company
  • Working knowledge of the MDD/MDR
  • High fluency in German, with very good spoken and written English
  • Experience working with ISO 13485 and conducting audits (internal or external considered)
  • Travel flexibility


Please apply with your CV or contact the job poster Rebecca Woodfield for further details on this opportunity and additional vacancies in Regulatory Affairs and Quality Management.

+44 208 638 5376