Description
Regulatory Affairs (Medical Devices) - £ plus benefits - LondonA global human care company who pioneer innovations and clinical solutions are looking for a regulatory affairs compliance engineer to join their expanding medical device division.
This role offers excellent career advancement and the opportunity to work with a world renowned company that will expose you to unique devices and provide you with the support necessary to progress in your professional development.
Responsibilities:
- Lead regulatory compliance planning
- Support the QA & RA department
- Proactively support the organizations product standard compliance
- Provide expertise on applicable standards to the business
- Participate and assist Notified Body audits, certification and other governmental responsibilities
Key Skills Required:
- 3-5 years Regulatory and Compliance experience within Medical Devices
- Ability to interpret, adapt & provide guidance on product regulation
- Experience of maintaining existing CE certification compliance
- Competent communicator who can communicate in a global multi-cultural environment
- Medical Device regulatory experience, specifically MDD 93/42/EEC, ISO 13485 and QSR 820
If you are interested in this position, please send an updated CV , or call for further details