Regulatory Affairs Associate (Medical Devices)

    Nottingham Permanent
  • 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

Kelly Percival
Quote job ref
Phone number
+44 1727 730 143

Job summary

Life Sciences
Regulatory Affairs
Healthcare / Pharmaceutical
Contract type
Consultant name
Kelly Percival
Consultant phone
+44 1727 730 143
Job reference