Regulatory Affairs Consultant
2 days ago
**Regulatory Affairs Consultant (Permanent) - Leading Medical Devices Consultancy - 100% remote (UK only) - £negotiable + pension, 25 days holiday + BH**:
A leading medical devices consultancy is now recruiting for a Regulatory Affairs Consultant to join them on a permanent basis.
**The Company**:
A leading medical devices consultancy who has been established over 25 years is now recruiting for a Regulatory Affairs Consultant to join them on a permanent basis. They’re well respected within the industry and work with a high number of medical device and IVD clients.
- Global Medical Devices Regulatory
- Offices in Warwickshire, however the role can be 100% remote
- Established over 25 years and highly respected in the industry and with notified bodies
- Lots of support, particularly around business processes enabling Regulatory Consultants to complete their work easier and faster
**The Role**:
The Regulatory Affairs Consultant is responsible for;
- Author and maintain clients Technical Files ensuring compliance to regulations
- Provide expert UK/EU and some US Medical Device Regulatory Consultancy to clients
- Review UK/CE technical files
- Work on multiple projects at any one point
**You**:
- An excellent understanding of European regulatory requirements for medical devices (essential) and IVDs (preferred)
- Authoring / writing technical files (essential) for a range of medical devices
- Pre and post approval experience
- Knowledge of CER writing is desirable but not essential
**What should you do next?**:
Carrot Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.
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