24.05.24 | Vollzeit | Basel (Basel-Stadt) | Gfeller Consulting & Partner AGOur client is a worldwide leader in design and manufacturing for the orthopaedic and medical device markets, including joint reconstruction, spine, trauma, sports medicine, extremities and dental. With world-class facilities located around the globe, they provide customers with an opportunity
Später ansehen22.05.24 | Vollzeit | Basel (Basel-Stadt) | Gfeller Consulting & Partner AGOur client is a worldwide leader in design and manufacturing for the orthopaedic and medical device markets, including joint reconstruction, spine, trauma, sports medicine, extremities and dental. With world-class facilities located around the globe, they provide customers with an opportunity
Später ansehen23.05.24 | Vollzeit | Basel (Basel-Stadt) | Gfeller Consulting & Partner AGOur client is a worldwide leader in design and manufacturing for the orthopaedic and medical device markets, including joint reconstruction, spine, trauma, sports medicine, extremities and dental. With world-class facilities located around the globe, they provide customers with an opportunity
Später ansehen24.05.24 | Vollzeit | careers.tecan.comPreferably in the medical device industry - Experience in designing complex test automation models - The ability to fluently speak and write English and preferably German skills - Experience in E2E Test Automation for Windows Desktop apps - ISTQB certification (Advanced Level - Test Automation) is a plus
Später ansehen23.05.24 | Teilzeit, Vollzeit | Solothurn, Zürich, Zug, Sort-e | Michael Page InternationalPublic Sector & Not for Profit 9 - Projekt Assistent (m/w) 8 - Finanzwesen 1 - Beratung, Strategie & Change management 8 - Beratung 7 - Corporate 1 - Healthcare & Life Sciences 8 - Biotechnologie 3 - Medical devices 2 - Regulatory Affairs 2 - Pharma-Industrie 1 - Engineering & Produktion 6 - Qualität
Später ansehen23.05.24 | Vollzeit | Vaud | Michael Page Internationaldevices About Our Client Our client is an international company specialized in medical devices. Job Description - Technical documentation writing management (for Europe & the US); - Involvement in the development and design of the company's medical devices; - Risk management, from the early life of each
Später ansehen20.05.24 | Vollzeit | Hays AGRichtlinien EN ISO 13485; Medical Device Regulation; Schweizer Heilmittelgesetz; Quality System Requirements (QSR) o Kenntnisse globaler regulatorischer Anforderungen von Vorteil o Fähigkeit zum selbständigen Erkennen, Formulieren und Lösen von komplexen Problemen und Sachverhalten wie auch deren praktischen
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