Regulatory Affairs Manager - Market Access - APAC/China (m/f/d)

Your mission

• You are responsible for identifying the regulatory requirements for approval in the region
• You develop and support approval strategies
• The provision of submission documents is one of your tasks 
• You provide strategic input for the development of assigned projects 
• You are the central point of contact for our subsidiaries and partners 
• Advising and monitoring normative requirements in the development process
• You will be responsible for the implementation of internal company training courses 
• You are responsible for informing stakeholders about approval changes, standards and their impact on our products at an early stage 

Your talents

• Completed scientific/technical studies or comparable training 
• Experience in the field of medical device approval 
• Initial expertise in the field of medical devices 
• Confident appearance in global project structures 
• Communicative and analytical skills 
• Independent and structured way of working 
• Very good knowledge of German and English