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Senior regulatory affairs

Posted 9 March by X4 Group Easy Apply Ended

Medical Devices / Regulatory / ISO13485 / Manchester / Senior / Technical Files

Location: Manchester / Cheshire

Duration: Permanent

Rate: £35,000 - £40,000

My client is looking for an experienced Regulatory affair in the medical device industry to join their successful team. Ideally the candidate will have 3 – 5 years’ experience working to the certification of ISO13485.

They are looking for a Senior Regulatory Affairs, to compliment the team, ideally with the following skills:

  • Auditing to ISO 13485 and FDA 21 CFR Part 820
  • Strong experience with technical files
  • To contribute to regulatory and quality project teams
  • To review technical data as part of a project team
  • To provide regulatory review and technical input Review of non-conformities

This is a brand-new requirement and my client is looking to fill the position as soon as possible. They are looking to line up interviews ASAP and will move quickly on the right candidate.

Send your CV to , or call Jessica Frost on for more information.

Medical Devices / Regulatory / ISO13485 / Manchester / Senior / Technical Files

Reference: 34651187

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