The medical information manager will be handing complex Medical information inquiries in second line. The main tasks include but are not limited to the following task areas: Ensur…
Coordonner les prestataires techniques pour assurer le bon fonctionnement des solutions En charge du support de niveau 2 Installation, configuration et maintient des logiciels mé…
Organiser la maintenance préventive et curative de l'ensemble du parc machine, des infrastructures et du bâtiment. Gestion d'une équipe composée de 3-5 techniciens. Élaborer des …
Chef de projet en contact direct avec les clients interne ou externe Définir, sélectionner, qualifier, valider et contrôler les performances des nouveaux équipements/processus, pr…
Superviser la facturation de l'activité stationnaire et ambulatoire de l'institution Collaborer étroitement avec les assureurs, les autorités cantonales et les autres unités du D…
Assistance Téléphonique Répondre aux appels et aux tickets d'assistance, en fournissant une assistance de niveau 1 et 2. Diagnostiquer et résoudre les problèmes techniques renc…
The selected candidate is responsible for ensuring that each individual batch has been manufactured in compliance with laws in force in the country of destination, in accordance wi…
Provide Regulatory strategies for projects as RA representative in cross-functional teams Responsible for regulatory Assessment on product changes Coordinate the preparation of r…
Maintain Instructions For Use (IFU) for our medical devices, ensuring compliance with regulatory standards. Register medical devices in various regulatory databases (e.g., GUDID i…
Support Regulatory Surveillance process with regards to local EU regulation(s); support RA intelligence and regulatory surveillance process Actively engage in process improvement …
Directs the preparation and coordination of comprehensive regulatory submissions for Medical Devices, ensuring compliance with local and international regulations and achieving com…
Support team members in creating CE Mark submissions and change notifications to our Notified Body (NB), including responding to regulatory inquiries Aid in the completion and upk…
Vigilance & complaint processes management ; Support in post-market surveillance activities ; Medical device data management, creation and maintenance of associated documentation…
Generate and lead site metrics reviews such as KPI reviews and Quality Data Reviews. Manage Local and Global Quality Reports and other metrics reviews as applicable. Coordinate t…
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