Michael is responsible for the development of Technolution’s services within Quality Assurance (QA) and Regulatory Affairs (RA), which is an area of continuous growth. Michael has extensive experience in developing medical devices and works primarily in the border area between R&D and QA, e.g. preparing QA strategy and documentation. In addition, he coordinates the cooperation with a number of associated specialists within both QA and RA.
Michael works as Project Manager for our client’s development teams as well as many of Technolution’s own projects.
As a Senior Partner, Michael will participate in the strategical work in connection with the development of Technolution’s skills, focusing in particular on the integration of R&D, QA and RA.
Michael is educated M.Sc. engineer and has more than 25 years’ experience in the development of medical devices, 20 years as Project Manager. He has been working for Technolution for the last 4 years.
“We have been working successfully to add new skills to Technolution in order to handle the entire development task of a medical device, including CE marking and FDA 510(k) approval. With the new structure, both the responsibility and the continued development of Technolution will be even stronger. I look forward to participating in this work.”