Regulatory Affairs Specialist - Medical Devices

My client is looking for a Medical Device RA specialist to help with an MDR project for 12 months on site in Leeds.

40 hours per week - on site in Leeds

£50-52 per hour

Must have a BS within scientific or related field

Essential skills;

- 6 years within a senior or lead position within RA

- Experienced in global regulatory submissions

- RA specialist

- ISO13485 2016 standards

- UK based candidate

- Be able to work with little to no supervision

Functional and technical competencies;

- Excellent written, verbal and communication skills

- Presentation skills

Position duties and responsibilities;

- Provide independent regulatory guidance to product development teams in strategic planning, pre-marketing, and related submissions for optimal timelines for new and modified product launches

- Lead the submissions of licenses and authorisation for maintenance of existing products, international reg, and dossiers

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

Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales