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- Excellent opportunity to join a Medical Care business that puts patients first
- Great opportunity to be apart of a dynamic team working on exciting projects
About Our Client
This is a fantastic opportunity to join a Medical Care business that puts patients at the heart of everything they do.
Job Description
- Perform registration of medical devices with MHRA
- To maintain Technical Documentation Files for devices in accordance with the requirements of the UKMDD for UKCA marking activities
- Handle regulatory dossiers to support product license applications and product license maintenance
- Support post market surveillance, preparing reports for the product range according to procedures
- Developing and maintaining a sound knowledge of European and UK regulatory legislation and guidelines to provide advice and expertise internally for matters related to our products
- To support companies regulatory planning, developing strategies for the product range in accordance with the UK requirements
- To support risk management activities and the life-cycle of marketed products
- Updating and reviewing of IFUs, packaging and labelling
- Will have ample opportunities to work on a variety of regulatory activities across a range of products including medicines
The Successful Applicant
Experience and knowledge on the regulatory framework & ISO 13485
What's on Offer
Excellent benefits package available
Salary up to 45K depending on experience
Contact
Kelly Percival
Quote job ref
JN-012022-5240278
Phone number
+44 1727 730 143
- Sector
- Life Sciences
- Subsector
- Regulatory Affairs
- Industry
- Healthcare / Pharmaceutical
- Location
- Nottingham
- Contract type
- Permanent
- Consultant name
- Kelly Percival
- Consultant phone
- +44 1727 730 143
- Job reference
- JN-012022-5240278
