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Regulatory Affairs Executive

£DOE | Surrey |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887463

Consultant

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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. 

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The Role

Regulatory Affairs Executive, £DoE, Surrey

 

The Company

Highly successful global pharma based in Surrey. They have clear, defined career paths and support career development / progression. Offering a great work/life balance and flexible working as well as a competitive basic salary and benefits package.

  • Global pharmaceutical company

  • Multiple therapy areas

  • Competitive package including flexible working

  • Certified top UK Employer

  • Excellent career progression opportunities

 

The Role

The Regulatory Affairs Executive will be responsible for;

  • Full end to end regulatory lifecycle

  • MRP / DCP National phases

  • MA Variation / Renewal Applications

  • NPD MA's

 

You

As a Regulatory Affairs Executive you will have following experience;

  • 2 years' experience in end to end regulatory affairs lifecycle (medicinal)

  • Regulatory Affairs experience within a pharma or generics company

  • DCP / MRP

  • Working on existing products as well as NPD

 

What should you do next?

This Regulatory Affairs Executive role won't be around for long! Give me a call or send me an email to find out more! 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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