A growing medical devices company in Kent is currently in need of an experienced regulatory affairs specialist who will be able to join at manager level.
This is a unique role as you will work on more than one medical device, due to this you will ideally have worked for a few different medical devices companies (on different types of devices), worked for a company that produces several different types of devices or worked for a notified body where your product knowledge is utilised.
This is a key role in the development of lifesaving and life-improving medical technology. You will work closely with the quality assurance and design teams, within an ISO 13485 environment.
It is expected that you would have a strong knowledge of quality assurance and regulatory standards within the UK and Europe. So, in-depth knowledge of ISO 13485, CE Marking other standards will be essential. This role will give you the chance to shape their strategy and processes while providing great opportunities for growth and development.
Undertaking internal audits will be important in this role so hopefully you have experience of this in your current role.
It is understood that you would most likely hold a degree within an engineering, design, medical or sciences background, however the industry exposure is more important than your education, for this role.
You will be rewarded with a challenging role that you will never get bored with, with a tailored package to suit your expectations.
For more information make an application now and one of our consultants will be in touch to talk through the details with 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.
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