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Regulatory Affairs Senior Specialist / Assistant Manager

£negotiable DOE plus 10% bonus and an extensive list of benefits | Yorkshire & The Humber |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:884553



Katie Goulbourn

Which team do you work in?
I work within the Drug Development team.

Which area do you specialise in?
I specialise in recruiting Junior to Director level Regulatory Affairs & Quality Assurance professionals within Pharma, Healthcare, Medical Devices and Animal Health. 

How do you keep up-to-date with the issues in your sector?
Speaking daily with clients and candidates keeps me on top of the latest industry trends and news, combined with regularly visiting relevant websites and reading articles.

What's your favourite film and why?
I absolutely love a good rom-com, my favourite would have to be The Holiday.

If you could invent one thing what would it be?
Trackable GPS microchips for cats and dogs - how has this not been invented yet!?


The Role

Regulatory Affairs Senior Specialist, salary negotiable depending on experience plus 10% bonus and an extensive list of benefits, Yorkshire

Following a site restructure, one of the world's leading pharma and healthcare companies have a number of great opportunities for experienced Regulatory professionals to join their Regulatory Affairs teams.


The Company

This is an exciting time to join an expanding, highly successful global pharmaceutical company based at their Yorkshire site. Ongoing site refurbishment with state of the art equipment and facilities including staff shop, canteen, subsidised coffee shop and dry cleaners

  • Excellent career progression potential, rewarding high performance and looking for the Managers of the future

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

  • Extensive list of employee benefits including 10% annual bonus, 10% contributory pension, family healthcare plan, 25 days annual leave, childcare vouchers, share schemes, initiatives and discounted products.


The Role

The Regulatory Affairs Senior Specialist you will be responsible for:

  • Mentoring and leading junior team members, with 2 direct reports

  • Having complete ownership of your own commercial projects and seeing them through to completion, allowing delivery of NPDs into a global market

  • Assisting the RA Manager with operational and strategic NPD delivery



The successful Regulatory Affairs Senior Specialist will be able to demonstrate:

  • A minimum of 3-5 years Regulatory experience which will include both NPD and some experience in post approval maintenance activities

  • EU medicinal experience

  • Experience seeing projects through to completion

  • Experience mentoring junior team members, leadership experience beneficial

  • An agile, dynamic and ambitious attitude, with the desire to progress into a management role


What should you do next?

This Regulatory Affairs opportunity won't be around for long! The closing date for applications is by the end of July, 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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