Description
My client, a leading Medical Device company in the south ofEnglandis now looking for 2 Regulatory Affairs Specialists to assist in a new project for 2013.A new project for 2013 means that there is now an urgent need for 2 Regulatory Affairs Specialists on a 1 year contract.
General Responsibilities assisting current regulatory affairs team with the following;
- Compliance.
- General Product Development.
- Regulatory Submissions.
- Technical file writing and reviewing.
- CE marking.
The department that is recruiting deals with the first half of the regulatory life cycle and they want someone who can help bring the product through to marketing.
Experience Required;
- 3-5 Years Regulatory experience within a medical device role.
- Experience working with technical files and gaining CE marking.
- Experience of regulatory submissions in theUK,EU,USA.
- Product development experience is a plus but not essential.
If you believe you have the relevant experience then please apply below or call Joseph on .
To find out more about Real please visit www.realstaffing.com