Anja Teichmann has extensive experience in quality management and regulated development environments. Her professional background lies in the food industry and laboratory settings, where she gained solid expertise in analytical processes, quality assurance and regulatory requirements.

She currently oversees Quality Management at the Zurich Hub for Drug and Device Development (ZH3D) at the University of Zurich. In this role, she leads the implementation of a quality management system in accordance with ISO 13485 with the goal of achieving certification and supports research and development teams in meeting quality and regulatory requirements for medical devices and in vitro diagnostics.

Her focus is on the pragmatic implementation of MDR and IVDR requirements, as well as on establishing robust quality management structures that support the translation of scientific innovations into clinical applications.

Anja Teichmann completed the MBA Lucerne programme at the Lucerne University of Applied Sciences and Arts (HSLU) and combines her experience in laboratory operations, quality management and regulatory affairs with business and strategic expertise.