24.05.24 | 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 | 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 ansehen22.05.24 | Vollzeit | Meilen | Stettler Consulting AGUnd Weiterentwicklung des Regulatory- und Medical-Teams - Aufteilung der Verantwortlichkeiten innerhalb der Abteilung Registrierung - Erstellung und Optimierung von abteilungsrelevanten Abläufen - Einreichen von Neuaufnahme- und Änderungsgesuchen (CTD und eCTD) - Erstellung/Aktualisierung von Modul 3 (CMC-writing
Später ansehen21.05.24 | Vollzeit | Schaffhausen | Randstad Schweiz AGAnd services to advance the health and well-being of people. Cilag AG is an international manufacturing company of the Janssen pharmaceutical division of the Johnson & Johnson Group and produces pharmaceutical and medical device products as well as active chemical ingredients (APIs) for global markets at its
Später ansehen20.05.24 | Vollzeit | Hays AGAnd audits Your profile o Apprenticeship or bachelor/master’s degree in Life Science o Experience in Information Technologyand regulated environment (GMP/GLP) o Experience as system administrator in Windows Desktop/Server o Experienced user of MS SQL will be of advantage o Fluent in German language (writing
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