Back to All Jobs...

Regulatory Affairs Senior Associate – Global Medical Devices Company – Cheshire OR Remote – £negotiable

The Regulatory Affairs Senior Associate is responsible for submitting and maintaining global regulatory approvals, to support regulatory submissions for new markets and maintaining registrations and licences in existing markets.

The Company

This is an exciting time to join an expanding, highly successful global medical devices company based at their site in Cheshire. They develop and manufacture their own products and have an excellent R&D capability ensuring they stay at the forefront of medical devices and associated technology.

  • Global, leading medical devices company 
  • Manufacture and register a range of high-quality devices as well as many more in the pipeline
  • At the forefront of medical devices, particularly within wound care 

The Role

The Regulatory Affairs Senior Associate will be responsible for;

  • Submit and maintain global regulatory approvals, supporting regulatory submissions for new markets and maintaining registrations and licences in existing markets.
  • Advising the business regarding any regulatory enquiries
  • Coordinate the preparation, review and submit timely responses to requests for additional information from regulatory authorities on product registrations.

You

To apply for this role as a Regulatory Affairs Senior Associate our client is hoping for someone with the following skills and experience;

  • Good regulatory experience within medical devices
  • Good knowledge of MDD/MDR
  • Good knowledge of ISO 134585
  • Ideally experienced in managing registrations in EMEA, LATAM & APAC (desirable not essential)
  • Science based degree

What should you do next?

This Regulatory Affairs Senior Associate – Medical Devices role is one not to be missed; it encompasses the opportunity to work in a marketing leading, global healthcare company. If you are interested in this role or want to hear about any other Medical Writing jobs, please get in touch.

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.

Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

Apply Now!

Job Consultant

Hayley Shayestehroo

Regulatory Affairs

Senior Consultant

hayley@carrotpharma.co.uk

01625 361072

Related Jobs

Regulatory Affairs

Principal Regulatory Writer - Full or Part Time

Permanent From £55,000
Regulatory Affairs

Regulatory Affairs Manager - Biocides

Permanent From £55,000
Regulatory Affairs

Senior Medial Writer - Regulatory/Clinical

Permanent From £35,000

Get The Resources You Need In The Candidate Hub