Regulatory Affairs Consultant | Berater (m/w/d) Regulatory Affairs

Job Summary

Join VDE, a leading European technology organization, as a Regulatory Affairs Consultant to shape the future of medical software and AI. In this role, you will advise clients and partners on regulatory matters concerning the approval of medical software and AI systems, taking responsibility for project planning, control, and implementation. You will act as an expert, building networks with professionals and sharing your knowledge through events, training, and publications. The ideal candidate will possess a relevant university degree, profound knowledge of Regulatory Affairs for active medical devices, particularly medical software and AI, and expertise in quality management, technical documentation, conformity assessment, clinical evaluation, and post-market surveillance. This position offers an opportunity to contribute to technological advancement and consumer protection within a dynamic, innovative environment.