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Regulatory Affairs - Post Approval Associate

£40k-£50k + bonus | Yorkshire & The Humber, South Yorkshire, North Yorkshire |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:886224

Consultant

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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!?

More

The Role

Regulatory Affairs - Post Approval Associate, £40k - £50k plus 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 annual bonus, 10% contributory pension, family healthcare plan, 25 days annual leave, childcare vouchers, share schemes, initiatives and discounted products.

 

The Role

This is a great opportunity for an experienced Regulatory Affairs Specialist / Associate / Senior Associate who is looking to take that step up into leadership. You will be responsible for:

  • All post approval maintenance activities for existing branded products within global markets

  • Managing 10-15 projects simultaneously to meet deadlines

  • Liaising with other functions within the company and stakeholder management

  • Supporting a team of 1-2 direct reports who will predominately be responsible for completing submissions and dossiers

 

You

The successful Regulatory Affairs Associate will be able to demonstrate:

  • A minimum of 3 years experience in a Regulatory Affairs Associate / Senior Associate role or similar

  • Experience of post approval maintenance within the EU market as a minimum

  • Global Regulatory experience advantageous

  • Experience within Medical Devices or healthcare preferred

  • An agile, dynamic and ambitious attitude, with the desire to progress through the company

  • The ability to manage several regulatory projects simultaneously

 

What should you do next?

This Regulatory Affairs opportunity won't be around for long! 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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