Ferenc Markus

Ferenc Markus is an accomplished professional with extensive experience in risk management and regulatory affairs in the medical device sector. Currently serving as a Riskmanager at Zytomed Systems GmbH since May 2022, Markus has previously held roles at Charité as a Consultant focused on MDR/MDD, ISO 13485, and Scrum, and at GrOwnValve as a QM/Regulatory Specialist. With expertise as an Auditor for active medical devices at TÜV SÜD Product Service GmbH, Markus has conducted audits adhering to ISO 13485 and MDD standards. Prior experience includes entrepreneurial efforts in heart valve procurement and substantial research in tissue engineering during a PhD at the Medical University of Vienna. Markus's early career involved research roles at the Ludwig Boltzmann Institute and Fachhochschule Technikum Wien, where significant contributions were made in medical device standards and quality management systems.