Minimum 10 years of full-time work experience in the medical devices (Not active or active medical devices) andrelated industry in at one or more of the following:
a) closely related industries and the workplace such as design, manufacturing, testing or use of the device
b) the application of the device technology and its use in health care services and with patients;
c) testing the devices concerned for compliance with the relevant national or international standards;
d) conducting performance testing, evaluation studies or clinical trials of the devices.
Work Experience with other Notified Bodies as Medical Device Directive /Regulations Technical documentation assessor is preferred.