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Regulatory Affairs Specialist

£Negotiable DoE | UK |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889695

The Role

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.



Hayley Shayestehroo

Which team and area do you work/specialise in?

I work in the Regulatory Affairs team and recruit for Regulatory Affairs professionals at all levels within Pharma, Medical Devices companies and Regulatory Consultancies

What are some of the typical roles you cover?

I cover Regulatory Affairs positions at all levels within Pharma, Medical Devices and Regulatory Consultancies, these typically include;

Regulatory Affairs Associate jobs, Regulatory Affairs Executive jobs, Regulatory Affairs Senior Associate jobs, Regulatory Affairs Manager jobs, Regulatory Affairs Senior Manager jobs, Regulatory Affairs Director jobs, Regulatory Affairs Consultant jobs, Regulatory Writer jobs and Medical Writer jobs.

What are the hot issues in your sector currently?

Within Medical Devices it is the transition from MDD to MDR in May 2020. A lot of medical device companies are hiring Regulatory professionals to prepare their company for the transition

What’s makes you #DistinctlyDifferent?

I take pride in getting to know my candidates on a personal level as well as professional. Changing jobs is a big decision for most people so I like to ensure I am placing my candidates in a role that not only matches their career aspirations but also suits their personal situation and key motivations.


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