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Regulatory Affairs Specialist

Job Field:
Regulatory and Drug Safety Jobs
Regulatory Affairs Jobs
United Kingdom
All England
Contract Type:
40,000 to 50,000 per annum
Salary Description:
£Negotiable DoE
Carrot Pharma
Job Ref:

Regulatory Affairs Specialist - Leading Medical Devices company - Home based - £Negotiable DoE

The Company

This is an excellent opportunity to join a highly successful, growing medical devices client who have offices in West Yorkshire however the role can be home based.

* Excellent career development/progression
* Autonomous role, with a variety of projects to work on
* Market leading, highly successful global company
* Home based role with some travel to their offices in West Yorkshire when required

The Role

As the Regulatory Affairs Specialist, you will be responsible for;

* Create technical files for a range of medical devices
* Perform gap analysis and revision of existing documentation to ensure compliance with MDR
* Respond to and internal or external regulatory affairs queries


As the Regulatory Affairs Specialist, you will have the following experience:

* Regulatory Affairs experience within medical devices
* Good knowledge of MDD and MDR
* UK experience
* Good knowledge of ISO 13485

What should you do next?

This Regulatory Affairs Specialist job is a great role and won't be around for long! So don't delay. If you are unsure and need some advice, give me a ring, otherwise just click apply, upload your CV and send, it's really that easy!

Unless otherwise stated, if applying for a job within the 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.

Closing Date:

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