Quality Manager - Medical Devices - ISO 13485 - Bedfordshire

Job description

Quality Manager – Medical Devices – ISO 13485 – Bedfordshire

A respected, established and growing medical devices company, based in Bedfordshire, are currently looking to add a new Quality Manager to their company due to company expansion. This Quality Manager will have responsibility for managing the quality management systems (QMS) to ISO 13485 standards.

The reason this company is expanding is due to the new technologies they are continually developing. Due to the fact they are developing new medical devices the role of a Quality Manager is of paramount importance. If the devises fail in quality assurance or regulatory affairs it could be a big hit to the company, due to this you will need to have a number of years experience in the management of ISO 13485 standards and ideally have set up and run QMS.

It would also be advantageous to have a good knowledge of regulatory affairs standards and IVDD knowledge, however ISO 13485 management and documentation is more important.

As this company is growing the chance of career progression is very high. Along with career development you will also be rewarded with an excellent salary and benefits package.

Ideally you will hold a degree within a medical devices, science, engineering or biotechnology focus, however experience managing ISO 13485 quality standards will be more important.

For more information please feel free to call Andre Welsh, Director of Medical Devices recruitment specialists Newton Colmore Consulting, on 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 Manager, Quality Assurance Manager, Quality Engineer, Quality Assurance Engineer, Medical Devices, ISO 13485, IVDD, QMS, Quality Management System, Medical Technology, Regulatory Affairs