A highly reputable and leading medical device manufacturer, we are currently partnered with are looking to expand their forever growing Regulatory team.
Regulatory Affairs Manager
Zug, Switzerland (Hybrid)
In this position you will be responsible for:
• Registering medical devices internationally
• Preparation and execution of Regulatory documents and technical files Creation and maintenance of technical documentation according to MDD/MDR
• Creation and maintenance of technical documentation according to MDD/MDR
• You will be responsible to monitor the international environment for standards and regulations.
• You will work in close collaboration with other departments like quality, development, production and product management.
You will bring:
• A scientific or relatable university degree
• Ideally some years’ experience within the Regulatory field
• Business fluent German & English
This company offer fantastic benefits with both internal and external training, 50% flexible home working and great opportunities for progression.
Please apply to hear more.