• Support and manage the creation of contracts and agreements with various authorities
• Ensure a solid and timely preparation of said documents in order to guarantee a steady flow of products throughout the entire distribution network and the availability to patients
• Consult regarding implications of changes in the legal environment and suggest as well as initiate adequate procedures


• Good understanding of the relevant legal framework as well as related documentation
• Foresee potential pitfalls and ensure stability of distribution chains
• Multiple years of experience within medical device regulatory affairs
• Fluency in English in both verbal and written form, German is a plus