Consultant, SAASCO Ltd.
I am Ilona Őzse, a quality engineer with more than a decade of professional experience in the field of medical devices. I started my career as a quality management manager, where I played a key role in the establishment, development and maintenance of quality systems. For the last three years, I have been working as a consultant for SAASCO, where I support our clients in developing, optimising and ensuring regulatory compliance of quality management systems, primarily tailored to medical devices.
My main area of expertise is the integration of quality management systems, in particular ISO 13485 and the requirements of the European Medical Device Regulations (MDR), into company processes. I am passionate about continuous improvement and regularly train myself on the latest standards and industry trends.
My commitment to additive manufacturing stems from the fact that this technology opens up new horizons in the medical device industry and offers efficient, personalised solutions for patients.
