31.10.19 | Vollzeit | Bern | DecomplixYou bring - a technical background and enjoy writing technical documents; - professional experience in quality management or regulatory affairs in the Medtech industry; - detailed knowledge of ISO 13485 and the certification processes for medical devices in Europe, ideally for software-only products
Später ansehen31.10.19 | Vollzeit | Bern | SPOUD AGYears of relevant experience in software development and the ability to write clean code - Know-how in state-of-the-art development frameworks, tools, and methods in your field of expertise - You like to work in a start-up environment but you feel comfortable also in the enterprise world - You have
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