Youssef Gannoune

* Adaptation of Hamilton’s portfolio of ventilators medical devices to the new regulatory requirements of IEC 60601-1:2005 /A1:2012 (3rd Edition) as well as the related collateral and particular standards (European / Harmonized standards for Medical devices, Directive 93/42/EEC) * Interface to external test houses (e.g. TÜV) for testing the compliance of the medical products according to the regulatory requirements * Establish and Update risk management documents according to EN ISO 14971:2012.

- Test management (medical devices) - Coordination, planning and controlling of the test activities of medical equipments (Hardware, Firmware, Software and Mechanics) during the development and integration phases of the products - Set-up and implementation of a test methodology - Project responsibility from test planning, test cases definition, test scripts implementation to the test execution - Identification, reporting and tracking of product defects - Release of test programs and regression flows

- Organizing trekking tours in the Atlas mountains and the Sahara - Organizing cultural tours in Morocco - Organizing information events about Morocco in Europe

Technical team leader product and test engineering.