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Regulatory Affairs Specialist (Medical Devices)

£Competitive salary and benefits package | North West, Lancashire |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887516

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 Specialist (Medical Devices) - Leading Pharmaceutical Company - Lancashire - £Competitive salary and benefits package

 

The Company

A fantastic company with a great reputation working across new and established medical devices. 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 will lead worldwide product registrations and CE marking activates to ensure timely and systematic approvals are made in accordance with regulatory and business requirements.

  • Regulatory lifecycle management and providing regulatory advice Supporting and coordinating regulatory approval for new products and changes to existing products

  • Ensuring that dossiers are created where appropriate in line with local country requirements (incl. CE mark and US).

  • Establish and maintain processes for maintenance of registrations.

 

You

As a Regulatory Affairs Specialist you will have experience in the following;

  • End to end regulatory lifecycle management within medical devices

  • Creating technical dossiers ready for submission

  • Strong stakeholder management

  • Global product registrations / CE Marking

 

What should you do next?

This Regulatory Affairs Specialist 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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