Eyal Hendel
About Eyal Hendel
Eyal Hendel is a Manager of Regulatory Affairs and Quality Assurance at Biosense Webster, with extensive experience in the healthcare industry and a strong background in program and project management. He holds multiple degrees from the Technion - Israel Institute of Technology and has worked in various roles related to regulatory affairs and medical device development.
Work at BioSense Webster
Eyal Hendel has been employed at BioSense Webster since 2017, initially serving as QA/RA Program Manager and currently holding the position of Manager, Regulatory Affairs and Quality Assurance. His tenure at the company spans over five years, during which he has been based in Yokneam Illit, HaZafon (North) District, Israel. In these roles, he has focused on regulatory affairs and quality assurance within the medical devices sector, leveraging his extensive background in the hospital and healthcare industry.
Education and Expertise
Eyal Hendel holds multiple degrees from the Technion - Israel Institute of Technology. He earned a Master's Degree in Systems Engineering from 2011 to 2013. Prior to that, he completed a Bachelor of Science in Biomedical Engineering from 2002 to 2005. Additionally, he obtained a Bachelor of Architecture in Architecture and Town Planning from 1997 to 2002. His educational background supports his expertise in regulatory affairs, quality assurance, and project management within the medical devices field.
Background in Regulatory Affairs
Eyal Hendel has a significant history of experience in regulatory affairs, having worked in various capacities within the healthcare and medical devices sectors. Prior to his current roles at BioSense Webster, he served as a Regulatory Affairs Leader for Product Surveillance at GE Healthcare from 2015 to 2017. He also held the position of Development Manager at AMIT - Alfred Mann Institute at the Technion from 2008 to 2014, and worked as a Medical Device R&D Engineer at MediGuide from 2005 to 2008.
Achievements in Project Management
Eyal Hendel possesses a strong background in program and project management, which is evident from his roles in various organizations. His experience includes overseeing regulatory affairs and quality assurance initiatives, as well as managing development projects in the medical devices sector. His skills in Good Manufacturing Practice (GMP) and nanotechnology further enhance his capability to lead complex projects effectively.
Skills in Verification and Validation
Eyal Hendel has developed expertise in Verification and Validation (V&V) processes specifically within the medical devices sector. This skill set is crucial for ensuring that medical devices meet regulatory standards and function as intended. His knowledge in V&V complements his roles in regulatory affairs and quality assurance, contributing to the overall safety and efficacy of medical products.