Regulatory Affairs Manager

My client is searching for a Regulatory Affairs Manager (m/f/d) for in vitro diagnostic medical devices ( IVD) who will focus on providing regulatory support for IVDs and companion diagnostics ( CDx) throughout the entire product lifecycle and will work on a wide range of tasks. This position offers hybrid working options and is open to 80–100% working hours.

Responsibilities:

• Ensuring compliance with EU requirements ( IVDD 98/79/ EC, IVDR 2017/746)
• Development and implementation of tailored solutions to meet regulatory requirements for a wide range o...
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