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Regulatory Affairs Executive (Clinical)

£Negotiable DoE | South West, Gloucestershire |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887738

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 (Clinical) - Medical Devices company - Gloucestershire, £Negotiable DoE

 

The Company

This is an exciting time to join an expanding, highly successful medical devices company based at their Gloucestershire site. They offer excellent training and development opportunities as well as great career progression opportunities.

  • Highly successful medical devices company with a range of devices in the market

  • Great benefits with bonus, pension, healthcare etc

  • Great career progression opportunities

 

The Role

As the Regulatory Affairs Executive (Medical Devices) - Clinical you will be responsible for;

  • Preparation of clinical assessment / evaluations as well as post market clinical follow up studies

  • Upgrade the company's clinical evaluation reports to comply with MEDDEV 2.7.1 Rev 4 and MDR 2017/745

  • Create PSURs

  • Assist the Regulatory Affairs Manager in creating and maintaining documents ensuring compliance to the MDR.

 

You

As the Regulatory Affairs Executive (Medical Devices) - Clinical you will have the following experience:

  • Knowledge of regulatory and legal requirements regarding Medical Devices

  • 1-2 years' experience in medical devices

  • Knowledge and experience of writing clinical evaluation reports is preferable

  • Relevant life sciences degree or equivalent

 

What should you do next?

This Regulatory Affairs Executive (Medical Devices) - Clinical 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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