Qa/Ra Manager

Regulatory Affairs Manager

South East

An exciting opportunity has arisen for a Regulatory Affairs Manager to join a globally successful Medical Device company at their head office in Oxfordshire. The main focus of the role will be to manage the company's Regulatory Affairs strategy and ensure they meet the relevant Regulatory requirements. Key responsibilities will include:

* Communicating with the MHRA and other regulatory bodies as appropriate.
* managing all aspects surrounding Regulatory Affairs, including the registration, CE Marking and release of Class 1 and 2 Medical Devices
* Provide technical support to manufacturing departments on regulatory issues and work closely with the quality department.

To apply for the role of Medical Device Regulatory Affairs Manageryou will have the following:

* BSc degree or equivalent in relevant subject area. .
* Previous management experience.
* Solid regulatory experience within a medical device environment.

If you believe you have the relevant experience, or you know someone who does, then please contact Joseph on 02077587322, or email on

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