Timothy Druyos is an experienced Principal Quality Systems Engineer at Boston Scientific, where responsibilities include managing sustaining activities for Class III permanent implants and contributing to compliance initiatives. Previous roles include Supplier Quality Engineer at Kestra Medical Technologies, Inc., and various positions at Boston Scientific, where Timothy specialized in design assurance and operational quality engineering. Expertise encompasses ISO 13485, ISO 14971, and 21 CFR Part 820 regulatory environments, with a focus on risk management, CAPA projects, and cross-functional collaboration. Timothy holds a Master of Science in Biomedical Engineering from the University of Minnesota and a Bachelor of Science in Biomedical Engineering from Purdue University.
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