University degree in a medical, scientific, legal or technical field with at least 3 years of professional experience in the relevant field (preferably with expertise in neurorehabilitation).
You have relevant experience with the quality management system for medical devices (ISO 13485) and the European Medical Device Regulation (MDR). In addition, experience in software for medical devices according to IEC 62304 and in risk management (ISO 14971) is an advantage. Ideally, you already have experience as a QMB and PRRC.
Very good German and good English skills.
You are characterised by analytical thinking and a very structured way of working. You are a team player and enjoy networking with interdisciplinary stakeholders. You are results-orientated and precise in the implementation of processes and documentation.