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Regulatory Affairs Manager

£Negotiable DoE | Yorkshire & The Humber |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887525

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. 

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The Role

Regulatory Affairs Manager - Medical Devices - £Negotiable, West Yorkshire

 

The Company

This is an exciting time to join an expanding, highly successful medical devices company in West Yorkshire.

  • Excellent career progression opportunities

  • Highly successful medical devices company

  • Great working environment and very competitive salary

 

The Role

The Regulatory Affairs Manager is responsible for;

  • Prepare and compile technical dossiers / documentation for CE and FDA review

  • Create technical files for Class I, IIa and IIb Devices

  • Prepare FDA 510K applications

  • Line manage a small team

 

You

  • Full lifecycle Regulatory Affairs experience within medical devices

  • Understanding of the Medical Device Directive

  • Experience with Class I, IIa, IIb Devices

  • Knowledge of Medical Device Regulation 2017/745/EEC requirements

 

What should you do next?

This Regulatory Affairs Manager 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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