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Head of Regulatory Affairs & Quality

Competitive salary and package | Cheshire |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887254

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

Head of Regulatory Affairs & Quality, £Negotiable, Cheshire

 

The Company

This is an exciting time to join an expanding, highly successful healthcare consultancy based at their new office in Cheshire. Offering consultancy and capability services to pharma companies in the UK & EU, this is a great role to be able own and define the day to day regulatory activities of the business.

  • Excellent opportunity to own and define the day to day regulatory activities

  • High profile and challenging role within the business

  • Great benefits with car allowance, pension, healthcare and share options

 

The Role

The Head of Regulatory Affairs & Quality is responsible for;

  • Manage a complex set of regulatory requirements across the business portfolio

  • End to end delivery of product dossiers and technical files

  • Reclassification applications for change of legal status (POM to P and P to GSL)

  • Regulatory intelligence

  • Own the quality management system

 

You

Extensive regulatory experience, currently at Manager / Senior Manager level and good experience dossier/technical file creation and registrations

  • UK / EU OTC experience

  • Excellent communication skills gained within a cross function role

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

  • Medical Devices experience would be beneficial as would Switch (POM to P or P to GSL)

 

What should you do next?

This Head of Regulatory Affairs & Quality 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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