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Lisa Heilemann finished her master’s degree in Biology Science in 2016. Since then, she has set up and performed validations on medical devices under ISO 19227, 11135, 11137 and 11607 for the cleaning, sterilisation and packaging of medical devices at Eurofins. Her core area of focus includes packaging and transport validation, aging studies, qualification of machines, microbiological monitoring / laboratory and systems for water treatment. She has excellent qualifications as an employee in the validation and quality assurance department. Since 2021, she has been a dual head, leading the validation department. Lisa Heilemann has been part of the DIN standards committee for the packaging and sterilisation of medical devices since 2022, where she shares her expertise and skills with other experts.