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Regulatory Affairs Consultant

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

Consultant

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Hayley Shayestehroo

Which team do you work in?

I work in the Regulatory Affairs team.

Which area do you specialise in?

I specialise in recruiting all levels of Regulatory Affairs professionals within pharma, healthcare and medical devices. 

How do you keep up-to-date with the issues in your sector?

Speaking to candidates is the best way to keep updated with changes in the market. I also like to read relevant industry press and relevant articles on LinkedIn. 

What's your favourite film and why?

Mrs Doubtfire - it's an all time classic and I pretty much know it word for word. I love a good thriller too, anything with a good twist at the end. Law Abiding Citizen with Gerard Butler is one of my faves. 

If you could invent one thing what would it be?

Pizza that makes you slim! 

What makes you #DistinctlyDifferent?

I love watching pretty much any sport. I play netball twice a week and come from a footballing family, so have been taught how to do kick ups (my record is 21 without hitting the floor!) Work wise, I like to think I get to know candidates on a deeper level and really understand their drivers and motivations for moving to another company. 

More

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

 

You

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.



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