Client Operations, QA/RA
Ketryx
Jenn Dixon leads quality and regulatory client engagements at Ketryx, where she provides coaching and support for clients wishing to adopt the best Software Medical Device practices. Jenn brings extensive expertise in quality assurance, regulatory affairs, and project management from previous roles in the MedTech industry with a proven ability to develop and apply best practices that optimize both teams and processes.
Prior to Ketryx, Jenn was Director of QA/RA at Omniscient Neurotechnology, overseeing global regulatory submissions, maintaining ISO 13485 compliance, and managing cross-functional teams in areas such as post-market surveillance and Good Machine Learning Practices (GMLP). Jenn also served as a Design Assurance Specialist and Technical Project Manager, where she excelled in risk management, audit readiness, and leading agile development teams to deliver innovative solutions.
Jenn began her career at Synaptive Medical, supporting ISO 13485 compliance transitions and leading UDI implementation. She holds a Bachelor’s degree in Engineering from the University of Toronto.
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Wednesday, May 14, 2025
10:15 - 10:45 CEST
Thursday, May 15, 2025
14:05 - 14:30 CEST