Natalie Dubs is an experienced Senior Regulatory Affairs Specialist at Cochlear since December 2014, focusing on the submission of Class III medical devices and software for EU MDR certification. Expertise includes translating cybersecurity requirements into technical specifications, project management for MDR compliance, and preparing technical documentation in accordance with regulatory standards. Prior roles at Cochlear involved sustaining engineering and project management for medical devices, as well as computer systems validation, establishing frameworks for compliance with various regulations. Earlier experience includes project engineering in industrial settings and verification engineering for medical technologies. Natalie holds a dual degree in Computer Engineering and Biomedical Engineering from UNSW, completed in 2006.
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