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Quality and Regulatory Assistant

£Negotiable DoE | Yorkshire & The Humber |  Quality and Supply Chain, Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:888736

Consultant

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James Jamieson

Which team do you work in?

Regulatory Affairs and Product Design

Which area do you specialise in?

I specialise in recruiting junior level Regulatory and Product Design roles

How do you keep up-to-date with the issues in your sector?

I find that speaking to the experts (the candidates themselves) is the best way to stay up-to-date with current affairs and develop my own sector knowledge. I also like to take some time each week to have a look through LinkedIn to see what people in the industry are talking about.

What's your favourite film and why?

I'm a big fan of the new(ish) Bond movies, so I'd have to say Spectre or Skyfall. Failing that anything with Adam Sandler in it.

If you could invent one thing what would it be?

I'd love to invent a device that could see into the future (or just at next week's winning lottery numbers!)

What makes you #DistinctlyDifferent?

I have always been a people's person and enjoy helping anyone in whatever way I can. I find a great deal of satisfaction in helping candidates to find their dream next role and playing my part in such a life changing process. 

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The Role

Quality and Regulatory Assistant - Medical Devices Company - Yorkshire - £Negotiable DoE

 

The Company

Located in West Yorkshire and with big plans for growth over the coming months, my client who cover a range of medical devices are striving to become a global leader in their respective field as they continue their pursuit of excellence across all areas. They can offer:

  • Fantastic training

  • Excellent career progression opportunities

  • On-site parking

 

The Role

In the role of a Quality and Regulatory Assistant, you will be responsible for;

  • Assisting with the implementation and management of the company quality system, product registration and CE marking

  • Carrying out internal and external audits as required

  • Monitoring and deal with customer complaints and non-conformances

  • Preparing and making changes to Internal Quality Check Sheets

  • Assisting in the management and compilation of technical files and regulatory agreements

 

You

The ideal candidate will have experience in the following;

  • Familiar with compiling Medical device technical files for EU CE marking

  • Understanding and processing document change requests

  • Processing of customer complaints including root cause analysis and corrective and preventative action

  • Good Communication skills

  • Strong team player

  • Attention to detail

 

What should you do next?

This Quality and Regulatory Assistant position is too good an opportunity not to find out more about! If you'd like to discuss the role in some more detail or have any questions, please don't hesitate to give me a call! Alternatively, just hit the apply button, upload your CV and send - it's as easy as that

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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