Regulatory Affairs and Quality Assurance Manager - South Cambridge
A growing medical devices company in south Cambridgeshire are currently in need of an experienced regulatory affairs and quality assurance manager, as their first hire to lead a newly created team to deal with post-Brexit regulation and quality standards.
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.
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. As new medical devices are being manufactured all the time you will always be working on something new rather than managing pre-existing regulatory affairs documentation.
Also, you will have an excellent starting salary, benefits package and career progression.
For more information, please feel free to call Matthew Lowdon, Director of Medical Devices recruitment and Scientific 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.
Medical Devices Regulatory Affairs Specialist, RA Specialist, Regulatory Affairs Manager, Quality Assurance, ISO 13485, CE Mark, CE Marking, FDA 510k, RA Consultant, RA Manager, Regulatory Affairs Consultant
You must be eligible to work in the UK. Learn more
- Agency: Newton Colmore Consulting
- Reference: NC-TW-746217
- Posted: 9th November 2020
- Expires: 7th December 2020