Description
My Client is looking for a Regulatory Affairs Consultant to help them with the CE Marking of Medical device Product.skills Needed Include:
- 10+years of Regulatory Background
- Extensive background with Class Ii and Class III devices/allograft/biologics
- Expert in CE Marking and directives
- Assisted in writing the active implantable medical device directorate
- has worked with large notified bodies
To find out more about Real please visit www.realstaffing.com