Our client is a Swiss established engineering company with focus on specification, development and industrialization of the systems with mechanical and electronic components for industrial and medical applications.
Optimizing and improving the Quality Management System according to the ISO 13485
Conducting quality audits, MDSAP and MDR
Preparing country-specific registration files for national and / or international registrations
Supporting the registrations and approvals of the medical devices
Reporting about the market insights and trends in the medical devices industry
University Degree or equivalent formation combined with the trainings in the field of quality management
At least four years of work experience in a similar position
At least four years of work experience in medical devices industry
Experience in FDA, MDSAP, MDR, CE, CFDA etc.
Excellent communication in German and English both verbal and written, any other language of advantage
Entrepreneurial spirit and target oriented personality
You will work in a collaborative and inclusive environment that values diverse perspectives and continuous learning, and provides industry-
leading benefits with opportunities for career growth. Are you willing to join a very dedicated team? To engage in the recruitment process, please be so kind to submit your CV via our website using the apply button.
In case you have any questions about this role, please do not hesitate to call me during CET office hours.
41 (0)58 233 35 06