Brian Roth
About Brian Roth
Brian Roth is a Principal Engineer at Teleflex in Reading, Pennsylvania, with extensive experience in process validation and design transfer for medical devices.
Current Position at Teleflex
Brian Roth serves as a Principal Engineer at Teleflex in Reading, Pennsylvania, United States. In this role, he leads initiatives in Design for Manufacture and Assembly (DFMA) within new product development. He also heads design transfer teams to ensure the successful transition of new medical devices from development into manufacturing facilities globally. Roth has extensive experience in process validation and plays a crucial role in introducing new processes at Teleflex.
Previous Experience at Teleflex
Before his current position, Roth worked at Teleflex as a Staff Validation Engineer from 2007 to 2019, a tenure lasting 12 years. During this period, he was involved in various validation processes, applying his expertise in ensuring the effective introduction of new processes. His long-term contributions in validation engineering have been instrumental in Teleflex's product and process development.
Career at Arrow International
Prior to his roles at Teleflex, Brian Roth dedicated 18 years to Arrow International, working as a Process Engineer in the Reading, Pennsylvania area from 1989 to 2007. During his time at Arrow International, he focused on various aspects of process engineering, gaining extensive experience that he later carried into his roles at Teleflex.
Educational Background in Engineering
Brian Roth holds a Master’s degree in Manufacturing Engineering from Lehigh University, which he obtained between 1991 and 1994. In addition, he earned a Bachelor of Science (B.S.) in Mechanical Engineering from Drexel University, completing his studies there from 1985 to 1989. His strong educational foundation has been integral in his roles across various engineering and validation positions.
Expertise in Process Validation and Design Transfer
Throughout his career, Roth has amassed significant expertise in process validation and design transfer, particularly within the medical device sector. He is highly skilled in ensuring that new manufacturing processes are validated and that new products transition seamlessly from development to production. His leadership in these areas has been central to the successful implementation of new medical technologies.