09.05.24 | Vollzeit | Sort-en-Chalosse | Michael Page InternationalDocumentation 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 device; - Review and approval of validation and verification documents; - Acting as Process Owner; - Contribution to internal
Später ansehen01.11.19 | Vollzeit | Lausanne | headcount AGdevices enable scientists to improve productivity and effectiveness. The company strives to accelerate research and discovery of new therapeutics. Our client is committed to the continual development of innovative solutions for life science applications. They are headquartered in Silicon Valley and have
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