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Regulatory Affairs Associate

£Negotiable DoE | Yorkshire & The Humber |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887658

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 Associate, Leading Medical Devices Company, Yorkshire, £Negotiable DoE

 

The Company

This is an exciting time to join an expanding, highly successful medical devices company based at their Yorkshire site. Excellent training and development opportunities as well as great career progression opportunities.

  • Excellent career progression opportunities

  • Idyllic location with plenty of free onsite parking

  • Great benefits with bonus, pension, healthcare etc

 

The Role

As the Regulatory Affairs Associate you will be responsible for;

  • Responsible for maintaining all technical files and regulatory documents

  • Provide accurate medical device regulatory and quality guidance to the rest of the business

  • To ensure products comply with ISO 13485

  • Preparation of documents for regulatory submissions

 

You

You will have the following experience:

  • 18m experience in Regulatory Affairs within medical devices

  • Working knowledge of ISO 13485

  • Experience in the compilation and review of Class I, IIa, IIB, III EU technical documentation for CE Marking is desirable

 

What should you do next?

This Regulatory Affairs Associate 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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