06.11.19 | Vollzeit | Flurlingen | Qmedics AG•Master’s degree in scientific discipline such as biology, chemistry, engineering or equivalent •5 - 10 years’ experience in general regulatory affairs, with at least 4 years of international regulatory experience •Profound experience with international medical device (class II & III) regulatory approvals
Später ansehen01.11.19 | Vollzeit | Zürich | headcount AGOf the company. You will serve as the company’s scientific point of reference for activities regarding marketing, market access and - when required - regulatory affairs. Furthermore, you will support new business development by providing scientific insights on the company’s portfolio and future assets
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