Doug Hull serves as the Principal Design Quality Engineer at TAE Life Sciences, where he leverages his extensive expertise in software, device, and system testing to ensure compliance with FDA and ISO standards in the medical device industry. Since transitioning from a contract role to...
Doug Hull serves as the Principal Design Quality Engineer at TAE Life Sciences, where he leverages his extensive expertise in software, device, and system testing to ensure compliance with FDA and ISO standards in the medical device industry. Since transitioning from a contract role to a full-time position in November 2021, Doug has taken on the critical responsibilities of Verification and Validation (V&V) Lead, overseeing all aspects of design verification and validation efforts. His role encompasses a comprehensive range of activities, including risk management, usability testing, and the meticulous authoring and maintenance of design control documentation.
Doug’s proficiency in quality assurance and quality management is complemented by his adeptness in agile methodologies, allowing him to implement process improvements that enhance product reliability and safety. His hands-on approach to systems engineering ensures that all design controls are rigorously applied, and he actively engages in requirements management to align project outcomes with regulatory expectations. Key projects under his leadership have involved the development of innovative medical devices, where he has successfully integrated usability engineering principles to enhance user experience while maintaining compliance with stringent industry standards.
With a strong foundation in system testing and a strategic focus on test strategy, Doug Hull is dedicated to advancing the quality and efficacy of medical devices at TAE Life Sciences. His commitment to excellence not only supports the organization’s mission but also contributes to the broader goal of improving patient outcomes through reliable and safe medical technologies.
