Quality Engineer - Cambridge - Medical Devices
A small and specialised medical devices company, based in Cambridge, are currently in need for a new Quality Engineer. You will be working alongside a number of different teams so you will work on multiple medical devices at once, meaning you will never get bored.
This role is focusing on new product development of medical devices, so hopefully you will have worked as a Quality Engineer on products that have been created from scratch. You will be responsible for maintaining ISO 13485 standards during the design and prototyping stages. It would be ideal if you have auditor qualifications also, but not essential.
Apart from ISO 13485 standards it would be ideal if you have strong knowledge of FDA 21 CFR 820, CAPA and auditing. Your role will be vital in the successful development of life saving projects, if you have design assurance knowledge also this would be highly advantageous.
If you do not have medical devices knowledge but do have pharmaceutical manufacturing knowledge you may still be considered as it is also a highly regulated field.
It is expected that you would hold an engineering degree but industry experience is more important. The wider the range of medical devices you have worked on, so consultancy work would be a bonus or working for a company that works on a range of different technologies.
You will be rewarded with an excellent salary, benefits package, career progression and skills training. If you want to work in a role that give you variety, test your skills daily and help with the development of life saving technologies 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.
Quality Assurance, Quality Engineer, Quality Assurance Engineer, ISO 13485, EN 60601, FDA 510k, FDA 21 CFR 820, Quality Auditing, Medical Devices
- Agency: Newton Colmore
- Posted: 15th February 2018
- Expires: 15th March 2018
- Reference: QECMD05