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Medical Devices Regulatory Affairs Specialist - Cambridgeshire

Cambridgeshire   •  Negotiable  •  Permanent, Full time

Medical Devices Regulatory Affairs Specialist - Cambridgeshire

Due to the growth of a technology leading medical devices company, based in Cambridgeshire, there is need for a new Regulatory Affairs Specialist to work with the companies R&D teams and their clients on the regulatory affairs standards advice on the creation of new products.

As you will be working with the R&D team it would be highly advantageous if you have knowledge of design assurance processes. This is not a role that is about filling out regulatory documents, this is a role where you will be very involved with the R&D team and providing vital advice on the creation of medical devices.

It is essential that you have medical devices regulatory affairs knowledge especially ISO 13485 and FDA 510k knowledge. The products this company have been developing are industry changing and will improve the lives of people around the world.

It is expected that you would hold a 1st or 2:1 degree within an engineering or sciences discipline along with a number of years experienced within regulatory affairs.

This is a growing company, due to this they offer career progression, excellent salary, benefits package and the chance to work on life improving devices.

So if you have strong regulatory affairs knowledge in the medical devices sector and are looking for a testing role then apply now.

For more information please feel free to call Andrew Welsh, Director of Medical Devices recruitment specialists Newton Colmore Consulting, on 0121 268 2240 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, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.

Regulatory Affairs Specialist, R&D, New Product Development, ISO 13485, Quality Assurance, Medical Devices Regulatory Affairs, FDA 510k, Regulatory Affairs FDA 510k, Medical Devices Recruitment

You must be eligible to work in the UK. Learn more

  • Agency: Newton Colmore
  • Posted: 14th March 2018
  • Expires: 11th April 2018
  • Reference: MDRASC05