Daniel Bowen
About Daniel Bowen
Daniel Bowen is a Quality Engineer with expertise in risk management and human factors engineering. He has worked for various organizations in the medical device and pharmaceutical sectors, focusing on product quality and regulatory compliance.
Current Role at Suvoda
Daniel Bowen serves as a Quality Engineer at Suvoda, a position he has held since 2024. In this role, he focuses on ensuring product quality and compliance with industry standards. His responsibilities include developing test methods and validation processes that align with regulatory requirements. He has been with Suvoda for 7 months, contributing his expertise in risk management and human factors engineering to enhance product safety and effectiveness.
Previous Experience at Kymanox
Prior to his current role, Daniel Bowen worked at Kymanox in various capacities. He served as an Associate Quality Specialist from 2021 to 2022 for 10 months, and as an Associate Engineer in Device Development & Commercialization from 2023 to 2024 for 4 months. Additionally, he held the position of Associate Quality Engineer from 2022 to 2023 for 1 year. His experience at Kymanox involved risk management and ensuring compliance with industry standards.
Emergency Medical Technician Background
Before transitioning to quality engineering, Daniel Bowen worked as an Advanced Emergency Medical Technician at Ashe Medics from 2018 to 2020 for 2 years. This role was based in West Jefferson, North Carolina, where he gained valuable experience in emergency medical services, which contributed to his understanding of human factors in medical device design.
Education and Expertise in Chemistry
Daniel Bowen earned a Bachelor of Science in Chemistry from Appalachian State University, completing his studies from 2017 to 2020. His educational background provides a strong foundation for his work in quality engineering, particularly in risk management and human factors engineering. He specializes in designing medical devices that accommodate human capabilities and limitations.
Regulatory Compliance and Post-Market Surveillance
In his professional career, Daniel Bowen has gained experience in preparing regulatory submissions and responses, ensuring compliance with governmental and industry regulations. He has also been involved in post-market surveillance activities, which include monitoring product performance and safety after market release. His focus on these areas supports the overall quality and safety of medical devices and pharmaceuticals.