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Regulatory Affairs Consultant (Contract) Med Dev

Regulatory Affairs Consultant (Contract) Medical Devices Hourly Rate

Medical devices client in the North West is looking for a regulatory affairs consultant for to work on technical files dossier and a commercial product which has now been re-classed as a medical device.

You will be;

- Working on the development, verification, validation of, and post-market support for the product.

- Regulatory submissions/registrations/compliance with US and EU

- Creating and reviewing Technical Files/CFR 820/21 part 11

- Make sure the product is fully compliant.

You MUST have experience with the above and extensive regulatory affairs experience within medical device companies.

Regulatory Affairs Consultant (Contract) Medical Devices Hourly Rate

Please contact Steven Ruddy from Real Staffing Group - Medical Devices on 0207 758 7322

To find out more about Real please visit www.realstaffing.com

15 February 2013
15 March 2013
RE-12453588
Steven Ruddy
Healthcare
Contract
Full Time
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