Medical Devices Regulatory Affairs Specialist - Birmingham

We Are SSG
07 Oct 2017
25 Oct 2017
Contract Type
Full Time

Medical Devices Regulatory Affairs Specialist - Birmingham

A growing Medical Devices company, based in Birmingham, are currently looking to add a Regulatory Affairs Specialist to their company to compile and submit regulatory affairs submissions for bodies across the globe.

Ideally you will be used to European submissions and FDA 510k submissions. However, if your focus has mainly been in Europe but you have a little knowledge of FDA 510k, we would still be happy to consider your application. So, if you have a desire to expand your knowledge of FDA 510k submissions this could be a great role for you.

The type of Medical Devices this company create and produce is closely linked to diagnostics, IVDD and biomedical technologies, so ideally you will have a scientific understanding rather than an engineering one. However, if you moved into regulatory affairs from an engineering background but have worked on regulatory submissions of diagnostics, IVDD or biomedical products we would still be open to your application.

This company's growth plans are very ambitious and has already been signed off, due to this I expect career opportunities to be more readily available with this organisation compared to others in the sector.

Apart from career progression and the opportunity to work on FDA 510k submissions you will also be rewarded with an excellent salary and benefits package. Interviews are already in process so if you are interested, you need to make an application now.

For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment specialists Newton Colmore Consulting, on + or make an application and one of our team at Newton Colmore Consulting will contact you.

Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.