06.11.19 | Vollzeit | Zug | headcount AGIncluding publications and clinical trial databases, and produce reports on the medical background, treatment guidelines, drug mode of action, and competitive product
Später ansehen01.11.19 | Vollzeit | | Liechtenstein | GlobalLogic Switzerland LtdHigh level code quality of his own and team member’s code quality. - Participate in requirement collections, competitive product study, market study etc., - Decompose design elements into structured code as per prevailing coding guidelines, preparation and execution of test cases and development
Später ansehen31.10.19 | Vollzeit | Zug | headcount AGManufacturing is a must for this role \ Demonstrated knowledge of cGMP-standard biologics manufacturing & guidelines and product lifecycle management \ Experience with commercial and/or clinical manufacturing in GMP environment \ Knowledge of conjugation or parenteral drug product formulations desirable
Später ansehen31.10.19 | Vollzeit | Bern | DecomplixDecomplix is a compliance partner that simplifies market access for medical devices. As a legal manufacturer, Decomplix goes beyond just consulting. Proven experts guide developers and manufacturers through the CE certification. In times of more stringent regulatory hurdles, this business model
Später ansehen29.10.19 | Vollzeit | | Liechtenstein | GlobalLogic Switzerland LtdEtc., ● Decompose design elements into structured code as per prevailing coding guidelines, preparation and execution of test cases and development of test codes or test harnesses. Trace back through code, design and resolve issues and bugs. ● Translate high level product description or requirement
Später ansehen25.10.17 | Vollzeit | Zürich | Deloitte AGIn an analytical manner with structured decision-making, guided by senior leadership feedback, to deliver implementable strategic recommendations for our clients Your skills and qualifications Your achievements in the previous steps of your career • Excellent academic achievements from a leading university
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