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Quality Management Engineer (26213)

Cambridge
£35k - £45k DoE + Top Benefits

Hey there! This is just one of many top career opportunities ECM can suggest — if this job isn't right for you, let us do the hard work! Tell us what you're looking for and we'll start searching for you. We promise to treat your CV as strictly confidential.

Quality standards support and development for medical device technology

Due to growth of the company and successful development of their key technologies, this scientific and engineering company are recruiting a Quality Management Engineer. The role reports to their Head of Quality, and will take responsibility of ensuring the company develops their quality processes and meet required quality standards for medical devices.

Requirements:

  • Background working in pharma, medical device or IVDR development sectors.
  • Knowledge and understanding of the following standards: ISO13485, FDA 21 CFR Part 820, Medical device 2017/745, IVDR, 2017/746 Regulation.
  • Relevant IT experience with electronic QMS systems.
  • Excellent communications (verbal and documentation) as well as time management and organisational skills.

This is a hands-on role, and is expected that the appointed person would work closely with scientists and engineers. Therefore most of the work will be onsite at their Cambridge offices and labs (although 1-2 days remote working is possible). In return, an excellent remunerations package is available.

Keywords: QMS Certification, ISO13485, 21 CFR 820, Program Management, Quality and Regulatory, Medical Devices, Cambridge / Hybrid Working

Please note: even if you don't have exactly the background indicated, do contact us now if this type of job is of interest - we may well have similar opportunities that you would be suited to. And of course, we always get your permission before submitting your CV to a company.

Recommend for £250 - see www.ecmselection.co.uk/tell-a-friend for details.