14-03-17 - Biomedical Sciences
In this function, you will be responsible for managing the regulatory aspects associated with our products and for setting up the clinical trial submission files.
28-02-17 - Quality Management
In this function, you will be responsible for the maintenance of the quality management system according to cGMP guidelines and support the translation of R&D projects to GMP standards.
ETH Zurich / University of Zurich