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Regulatory Affairs Manager

£Competitive salary plus car allowance, bonus and benefits package | South East, Buckinghamshire |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:886901



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. 


The Role

Regulatory Affairs Manager (Centralised procedures) - Leading Pharmaceutical Company - Buckinghamshire - £Competitive salary plus car allowance, bonus and benefits package


The Company

A fantastic company with a great reputation working across established and novel pharmaceutical brands. They offer unique development opportunities and support people to further their career in the UK or globally.

  • Innovative, ideas based company

  • Strong heritage in science

  • Culture of caring both internally and for patients

  • Agile and dynamic despite being a large corporation


The Role

This role supports centralised procedures for specific product portfolio; gaining approval of new indication, variations and other lifecycle procedures. It also offers the opportunity to work on the development of two early phase drugs.

  • Lead projects on labelling, PSURs, variations and other maintenance activities.

  • Input into PIP procedures and scientific advice packages for early phase drugs

  • Liaise with Regulatory agencies and local operating companies



Will have a solid regulatory affairs experience in centralised procedures, labelling, variations and maintenance activities. Plus, you need to be dynamic, proactive and flexible with strong communication skills.


What should you do next?

This Regulatory Affairs 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.

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