Reg Consultant Medical Devices £45ph Home working

04 Apr 2013
02 May 2013
Steven Ruddy
Full Time

My client is a global clinical trials client look to bring in a SME Regulatory Affairs consultant to work on registrations on within the medical devices team. The Regulatory Affairs contract will initially be for 3 months and will be reporting into the Technical Director.

The ideal candidate MUST have experience of;

5+ years experience in medical devices organisation.

Experience of registrations into Europe with Class II devices

Submissions into EU

Experience of MHRA and FDA

Must have experience of writing technical files for Class I, II, III products and achieved CE mark.

Regulatory Affairs Consultant Medical Devices Home/office based £55 - £60ph Immediate Start

Please contact Steven Ruddy from Real Pharma on 0207 758 7322

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