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Quality Systems Coordinator / England

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Location: Cambridge, England
Quality Systems Coordinator - Medical Device - Cambridge - Permanent

A new role has come available for a Quality Systems Coordinator to join an exciting and expanding Medical Device company in Cambridge. Do you have experience in project or QMS systems management and are interested in the opportunity to challenge yourself in a fast paced and progressive environment?

Quality Systems Coordinator Responsibilities:

  • Supporting, developing and maintaining the document and quality management systems
  • Management of live files, logs and information in thew Electronic Document Management System (EDMS)
  • Tracking, monitoring and reviewing actions to be completed on the QMS
  • Creating and reviewing SOPs
  • Ensuring that the QMS following ISO 9001 and ISO 13485
  • Support QMS improvement projects
  • Active member of the Quality Audit team
Quality Systems Coordinator Requirements:

  • Experience working in a regulated environment (ISO9001 or ISO13485)
  • A knowledge and development or manufacturing processes
  • Organised with a high attention to detail
  • Good knowledge of MS office and IT skills
In return you can expect a generous and salary and package including flexible working and share options as well as the opportunity to have an impact and progress your career. Please apply or contact me for more information.

How to Apply

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