Philips
Douglas Roberts is a seasoned professional with extensive experience in regulatory project management and quality engineering within the medical device industry. Currently serving as a Senior Regulatory Project Manager and Senior Design Quality Engineer at Philips since January 2017, Douglas has successfully led cross-functional teams in risk management for Sleep and Respiratory Care products and was the lead Design Quality Engineer during a major recall. Previous roles include Regulatory Associate at Bayer and project management positions at the Wallace H. Coulter Foundation and the University of Pittsburgh Innovation Institute. Douglas holds a Master’s Degree in Biomedical/Medical Engineering from the University of Pittsburgh and a Bachelor of Science in Biology from the University of Pittsburgh-Johnstown.
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Philips
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Philips' main purpose is to improve the health and well-being of humankind through innovation. Philips' goal is to improve the lives of 2 billion people by 2025, including 200 million in underserved communities. In 2021, Philips has over 1.8 billion euros invested in R&D and over registered 57,000 patent rights. When it comes to innovation, Philips aims to not do it in isolation - instead, they partner with healthcare providers, start-ups, universities (especially university hospitals), and other companies. Philips has been named by Boston Consulting Group in 2020 as the number 1 MedTech company in the world.