Sabine Nieba

Sabine Nieba has a diverse background in quality management and regulatory affairs in the medical device industry. Sabine is currently a Partner and COO at QUAREGIA - Quality & Regulatory Compliance, where they specialize in providing services for CE Marking, international product approvals, risk management, and project management. Additionally, they are a Special Coach for Innosuisse, focusing on regulatory affairs and cybersecurity. Sabine also worked as an Expert Regulatory Affairs at Berner Fachhochschule BFH and as a Competence Cluster Lead and Senior Consultant at confinis, where they provided advice and services to medical device manufacturers. Prior to that, they were an Expert Reviewer for Medical Devices at QS Zürich AG Zertifizierungen. Sabine has also held various roles at Sentec and Metrohm, including Member of the Executive Board, Head of Regulatory Affairs and Quality Assurance, and Project Manager R&D. Sabine'sexperience spans software development life cycles, technical documentation, and project management.

Sabine Nieba obtained their Diploma in Biochemistry from The University of Freiburg, where they studied from 1987 to 1993. Sabine then pursued their PhD in Biochemistry, Biophysics, and Molecular Biology at the University of Zurich from 1993 to 1997.