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Lise Skytte Brodersen

Consultant

Design Control
GMP
MDD/MDR
Project Coordination
Medical Device

Lise holds a BEng in Healthcare Technology from Aarhus University and has three years of experience in the industry of Medical Devices as a consultant.

Lise has worked as a Design Control Specialist where management and preparation of design control / technical documentation were the focus area. As a Design Control Specialist Lise has achieved extensive knowledge of the different development phases as well as the regulatory requirements that apply to the development of medical devices. Lise has also been the primary person and deeply involved in a Remediation Project supporting a multinational medical device manufacturer, where the purpose was to detect deficiencies in the design control documentation of legacy products as compared to current regulations and standards, including update of this documentation to achieve future compliance with the Medical Device Regulation (EU MDR).

As a consultant Lise is service minded. She strives for good and effective results where quality is in focus. Lise works analytically, systematically and cares for the detail.

“I like challenges, and my curiosity drives me. I am hardworking, energetic and take pride in performing my work with great precision and a high level of quality. I like to be well prepared and punctual. I believe in the open dialogue, where honesty, knowledge sharing, and cooperation brings us closer to the goal together”.