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
