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Regulatory Affairs Senior Associate

£Negotiable DoE | Yorkshire & The Humber |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:888168

Consultant

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James Jamieson

Which team do you work in?

Regulatory Affairs and Healthcare Communications

Which area do you specialise in?

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

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

I find that speaking to the experts (the candidates themselves) is the best way to stay up-to-date with current affairs and develop my own sector knowledge. I also like to take some time each week to have a look through LinkedIn to see what people in the industry are talking about.

What's your favourite film and why?

I'm a big fan of the new(ish) Bond movies, so I'd have to say Spectre or Skyfall. Failing that anything with Adam Sandler in it.

If you could invent one thing what would it be?

I'd love to invent a device that could see into the future (or just at next week's winning lottery numbers!)

What makes you #DistinctlyDifferent?

I have always been a people's person and enjoy helping anyone in whatever way I can. I find a great deal of satisfaction in helping candidates to find their dream next role and playing my part in such a life changing process. 

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The Role

Regulatory Affairs Senior Associate - Medical Devices, Global Health & Hygiene Company, Yorkshire, £Negotiable DoE

 

The Company

This is an exciting time to join an expanding, highly successful global healthcare company based at their Yorkshire site. Fantastic refurbished offices with many facilities including staff shop, canteen, subsidised coffee shop and dry cleaners.

  • Excellent career progression opportunities

  • City location with plenty of free parking onsite and close to major transport links

  • Great benefits with bonus, pension, healthcare, share scheme and discounted products

 

The Role

As a Regulatory Affairs Senior Associate - Medical Devices, you will be responsible for;

  • Creating technical files/dossiers in preparation for submission to relevant bodies

  • Providing support to the Global Regulatory Health teams in the medical device dossier creation process and/or variations to existing dossiers.

  • Collaborating with the Global Regulatory Health teams to help define and mitigate key risks identified on any data proposed for inclusion in the dossier

  • Maintaining technical files and regulatory documentation for medical devices

 

You

As a Regulatory Affairs Senior Associate - Medical Devices, you will have the following experience;

  • Regulatory Affairs experience, ideally within medical devices

  • Life Sciences degree

  • Full life cycle regulatory experience

  • NPD experience is preferred, but not essential

 

What should you do next?

This Regulatory Affairs Senior Associate - Medical Devices role is too good an opportunity not to find out more about! If you'd like to discuss the role in some more detail or have any questions, please don't hesitate to give me a call! Alternatively, just hit the apply button, upload your CV and send - it's as easy as that!

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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