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RA Consultant Medical Devices Home based £55 ph Immediate Start
The client is a global trials client they're looking for a 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 intoEuropewith 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.
It would also be beneficial to have experience with OTC products.
Regulatory Affairs Consultant Medical Devices Home/office based £55 - £60ph Immediate Start
Please contact Steven Ruddy from Real Pharma on 0207 758 7322
To find out more about Real please visit www.realstaffing.com