Carl Zeiss Meditec
Laura Bourdin currently serves as the Quality and Regulatory Affairs Manager at ZEISS Medical Technology, a position held since April 2019. Prior to this role, Laura held the position of Assistante QSE at ZEISS Group from October 2017 to March 2019, where responsibilities included the implementation of radiation safety management systems and ensuring compliance with CEFRI E certification. Earlier experience includes an internship in control at the Institut de Recherche Criminelle de la Gendarmerie Nationale, focusing on polymer studies and analytical methods. Laura holds a Master’s degree in Control and Quality from CY Cergy Paris Université and has specialized education in regulatory affairs for medical devices from Université Paris Cité.
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Carl Zeiss Meditec
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Carl Zeiss Meditec is a Germany-based medical technology and device company. It offers offers complete solutions to diagnose and treat ophtalmic diseases, visualization solutions for microsurgery and other technologies, such as intraoperative radiotherapy. The Company operates in two segments: Ophthalmic Devices and Microsurgery. The Ophthalmic Devices segment comprises activities in the area of ophthalmology, such as intraocular lenses, surgical visualization solutions and medical laser and diagnostic systems. The Microsurgery segment includes activities of neuro, ear, nose and throat surgery, as well as the activities in the field of intraoperative radiation. The Company has various production sites in Europe, the United States and Asia.