Sofie has 12 years of experience within design control for medical device development and life cycle management. Her work has spanned, requirement engineering, verification activities, documentation, QMS processes and MDR implementation. She has worked in executing roles, coordination roles, in support functions and as independent reviewer. She has a strong analytical mind-set, and is good at breaking down complex problems into manageable tasks. She works systematically by understanding requirements and dependencies to a task, subsequently working into the details. She is curious by nature and a fast learner which enables her to work independently as well as proactively. She thrives with working in a team and enjoy the collaboration with team members and stakeholders to reach a common goal.