Regulatory Affairs Specialist (Medical Device) £50phWest Sussex

Regulatory Affairs Specialist (Medical Device) £50phWest Sussex- Immediate Start

Following expansion, this market leading organisation now seeks to recruit a Regulatory Affairs Specialist (Medical Devices). The exciting opportunity is for an experienced Regulatory Affairs Specialist with a background in medical devices to join a market leading supplier of sophisticated radiotherapy and oncology medical systems.

Responsibilities include:
- To specifically provide a centre of competence for:
- Developing and maintaining US Food and Drugs Administration (FDA) regulatory knowledge, preparing and submitting 510(k) submissions;
- To proactively support the organization in achieving the necessary regulatory submissions needed for targeted market areas.
- To develop and maintain worldwide regulatory knowledge in the preparation of regulatory submissions and registrations
- Developing and maintaining Canadian Medical Device Regulation knowledge, preparing and submitting device submissions.

Must have experience of classes and technical files for Class I, II, III products and achieved CE marking.

Regulatory Affairs Specialist (Medical Device) £50phWest Sussex- Immediate StartTo find out more about Real please visit www.realstaffing.com