Founded in 2024, Madsen Quality Consulting specializes in Quality Management, Quality Assurance (QA), and Supplier Quality Management, with a focus on the medical device industry. We provide expert support in developing robust management systems, streamlining QA processes, and enhancing supplier quality management, ensuring compliance and operational excellence.
Whether your company requires additional resources or strategic guidance, we offer solutions to meet your quality needs.
Hans Georg Madsen
With over 30 years of experience in quality management, Hans Georg Madsen brings a wealth of knowledge and leadership to the consulting firm. Originally trained as a chemical engineer, Hans transitioned into quality management in 1994 with the release of ISO 9001’s second edition.
Hans’ career spans various industries, beginning with packaging in the 1990s and moving into medical packaging and medical devices at the turn of the millennium. His extensive background includes roles in Quality Assurance (QA), Quality Control (QC), and Regulatory Affairs (RA), working with critical processes from development to production.
He has led quality initiatives in globally recognized companies such as Demant, Thermo Fisher Scientific, Coloplast, and Superfos Packaging. His ability to work with all levels of an organization, along with his international experience, ensures comprehensive and effective quality management solutions.