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Regulatory & Quality Manager

£Negotiable DoE | West Sussex |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:888535

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. 

More

The Role

Regulatory & Quality Manager, Leading Medical Devices Company, West Sussex - £Negotiable DoE

 

The Company

This is an exciting time to join an expanding, highly successful medical devices company in their offices in West Sussex. They offer excellent training and development opportunities as well as great career progression opportunities.

  • Excellent career progression opportunities

  • Great training and development

  • Exciting and innovative product range

 

The Role

As the Regulatory & Quality Manager, you will be responsible for;

  • Compiling and maintaining technical files for submissions in the EU, US and Canada

  • Post market surveillance

  • Ensuring compliance with MDD 93/42/EEC Medical Devices Directive, FDA and CMD Regulations

  • Managing and maintaining the QMS

  • Ensuring compliance with ISO 13285

 

You

As the Regulatory & Quality Manager, you will have the following experience:

  • Hands on Regulatory or Quality experience within medical devices (ideally both)

  • good knowledge of MDD 93/42/EEC

  • Good knowledge of ISO 13485

  • Management experience is preferred however not essential

 

What should you do next?

This Regulatory & Quality 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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