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Regulatory Affairs Associate Manager

£Competitive salary and benefits | Yorkshire & The Humber |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887156

The Role

Regulatory Affairs Associate Manager - £Negotiable, Yorkshire

 

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 onsite parking and close to major transport links

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

 

The Role

The Regulatory Affairs Associate Manager is responsible for;

  • Managing, defining and implementing the regulatory strategy for assigned projects

  • Project management of Regulatory NPD requirements and dossier / technical file creation

  • End to end delivery of product dossiers and technical files

  • Achieve market registrations and launches

 

You

Extensive regulatory experience, currently at Senior Associate / Associate Manager level and good knowledge in NPD and dossier/technical file creation and global registrations

  • EU / Global OTC devices experience is essential

  • Excellent communication skills gained within a cross function role

  • A high level of self-motivation and drive, with proven visible success

 

What should you do next?

This Regulatory Affairs Associate 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.

Consultant

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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 is your greatest fear?

I don’t really have one, but if there’s one thing I’m well not keen for it would be snakes or an army of ants…

 

How would your friends describe you in three words?

Funny, healthy, sporty

 

You’re stranded on a desert island – what one thing could you not live without?

Bear Grylls! He’d have us rescued in no time!

 

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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