Academic Work Switzerland SA is seeking a Regulatory Affairs Specialist in Etoy, Switzerland, to oversee regulatory compliance and product lifecycle for medical devices. This role involves collaboration with R&D and Marketing teams globally. The ideal candidate has experience in regulatory affairs within the medical device industry, advanced knowledge of Medical Device Regulation (MDR), and fluent English communication skills. J-18808-Ljbffr
Global Mdr Regulatory Affairs Specialist – Medical Devices
ACADEMIC WORK SWITZERLAND SA
Etoy, Waadt
Veröffentlicht vor 4 Tagen
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