Description
My client is one of the leading companies within the medical devices industry.Currently they are looking for a regulatory affairs consultant for 7 month project.
Start: Immediately (4days a week)
Duration: December 2014
Location: Switzerland
Requirements:
- EU US RA Background
- Strong design control knowledge
- Medical devices experience (Implants, Orthopaedics is an advantage)
- Experience with process/product change management
- Fluent English, additional German is a big advantage
Task (not limited to):
- Legacy review of design history documents
- Provide regulatory inputs to the remediation team
- Review of product label contents
- Develop strategies for implementations of product warning and warning label changes into the technical documentation (incl. Risk files)
If this sounds like an interesting opportunity for you, I am looking forward to hearing from you.
<p>To find out more about Real please visit <a href="http://www.realstaffing.com">www.realstaffing.com</a></p>