Grégoire S.

Ingénieur Recherche/développement at Debiotech SA

Grégoire S. is currently working as an Ingénieur recherche/développement at Debiotech SA since October 2023. Prior to this, Grégoire worked as a QA automation engineer at Pix4D from July 2021 to August 2023. Grégoire's background includes experience as a Postdoc at Ecole polytechnique fédérale de Lausanne, where Grégoire collaborated on various projects related to IoT features for mechanical watches and neural network training. Grégoire holds a PhD in Low Power Sensing and Processing in Wearable Biomedical Devices for Personalized Health Monitoring and a Master's degree in Electrical, Electronics, and Communications Engineering. Grégoire also has experience in android app development, advanced mechatronics, and quality control in a cleanroom environment.

Location

Lausanne, Switzerland

Links

Previous companies


Org chart

This person is not in the org chart


Teams

This person is not in any teams


Offices


Debiotech SA

For over 30 years, we have been developing innovations for MedTech. Through the various medical devices, we have designed and licensed, we have developed unique skills and expertise. It is therefore quite natural that we have chosen to share our entrepreneurial experience to accompany your developments. From the idea to the marketing of an innovative and compliant medical device (FDA 510k and/or CE marking), we are at your side. What we offer 1/ Research & Development: we take care of your technical development (software, mechanics, and electronics) while advising you. 2/ Compliance: we accompany and guide you in the management of your project within the framework of a compliant medical device development process (eg. preparation of technical files for clearance submission). We follow the same goal: Improving patient’s lives together. Facts & figures: - over 20 different medical product developments (drug delivery, artificial organs, nephrology, cardiology, diabetes, …) - over 40 license agreements - numerous prestigious awards - more than 500 granted national patents - ISO 13485 certified QMS and following FDA 21 CFR Part 820 requirements - compliance with MDR regulations and requirements of ISO/IEC 62304, 60601-1, 62366, 14971, …


Employees

11-50

Links