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