Regulatory Affairs Contractors X2

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 02077587322.To find out more about Real please visit www.realstaffing.com