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Regulatory Affairs Consultant

£Negotiable DoE | Yorkshire & The Humber |  Regulatory Affairs, CRO, Regulatory Consultancy |  Permanent  | Ref:887369

The Role

Regulatory Affairs Consultant, Regulatory Consultancy, West Yorkshire, £Negotiable DoE


The Company

This is an exciting time to join an expanding, highly successful regulatory consultancy based at their West Yorkshire site. They offer excellent training and development opportunities as well as great projects to work on and manage.

  • Highly successful regulatory consultancy with a range of leading clients

  • Great projects available to manage

  • Great career progression opportunities


The Role

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

  • Manage various regulatory and some quality focused projects

  • Liaise with clients and relevant bodies when compiling and preparing submission documents

  • Create and maintain technical dossiers in preparation for submission



As a Regulatory Affairs Consultant, you will have the following experience:

  • Good background in Regulatory Affairs either with Pharma or Medical Devices

  • Good hands on experience of technical dossier creation and submission

  • Strong stakeholder management be able to liaise with various teams within the business as well as external clients

  • Science related degree

  • Good project management skills


What should you do next?

This Regulatory Affairs Consultant 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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