Four years experience in design control and requirements management for complex medical systems with ambitious project timelines.Well versed in medical device regulations such as 21 CFR part 820 and ISO 13485.Proven ability to drive real change in large organizations through collaboration, clear and timely communication, and empathy.Strong materials science background with a deep understanding of fracture mechanics, microstructure-property relationships, electrochemistry and production processes.Expert in product verification with hands-on laboratory experience in diverse industries such as performance coatings, renewable energy, and injection-molded medical devices.