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Regulatory Affairs Specialist

This job is no longer available

Real Staffing
08 April 2013
06 May 2013
Joseph Dykes
Contract Type
£45 - £55 per hour

Further information

General Responsibilities include;

  • Directing and advising team on their regulatory procedures on the new medical device project.
  • Writing and developing Medical Device Technical files.
  • Maintaining Contact and submitting relevant documentation to the MHRA and FDA.
  • Leading project from its current position through regulatory submissions, right through to product registration.

Key skills needed;

  • 5+ year's regulatory experience of Regulatory Affairs within a medical device environment.
  • Ability to display and advise on regulatory requirements to ISO 13485 standards.
  • Familiar with submission within theUKandUSAis essential; EU would be beneficial but not essential.
  • Experience of leading projects would also be a bonus but not essential.
  • Experience of active medical devices is a strong requirement.

Other Information

  • Working from home is something that this role will also allow as long as 2 days on site can be achieved.

My client is looking to move fast so if you believe you are suitable or know of someone who is please contact Joseph.

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Real Staffing

Real is a global leader in the provision of pharmaceutical, biotechnology and medical devices recruitment services.