Yonit Ringel
About Yonit Ringel
Yonit Ringel is the Principal Regulatory Affairs Specialist at Boston Scientific, with extensive experience in regulatory affairs and quality assurance for medical devices.
Title
Yonit Ringel is currently the Principal Regulatory Affairs Specialist at Boston Scientific.
Company
Yonit Ringel currently works at Boston Scientific as a Principal Regulatory Affairs Specialist, based in Israel.
Professional Experience at Boston Scientific
Since 2023, Yonit Ringel has been serving as the Principal Regulatory Affairs Specialist at Boston Scientific. In this role, she focuses on regulatory matters related to medical devices, ensuring compliance with global standards and regulatory requirements.
Previous Roles in Regulatory Affairs
Yonit Ringel has extensive experience in regulatory affairs and quality assurance across several renowned companies. She worked as VP of RA/QA at The FixNip™ Medical Devices for 11 months (2022-2023), Head of Quality Assurance and Regulatory Affairs at Igentify for 1 year (2021-2022), and Regulatory Affairs Leader at GE Healthcare for 3 years (2018-2021). She also held the role of Design Quality Leader at GE Healthcare from 2015 to 2018.
Early Career Positions
Earlier in her career, Yonit Ringel has served in various roles: Design Quality Engineer at Philips (2013-2015), Consultant at Deloitte (2012-2013), PO at Orantech (2010-2012), and Test Engineer at Intel (2007-2010). These positions helped her build a solid foundation in quality assurance and regulatory affairs.
Education and Qualifications
Yonit Ringel holds a Bachelor of Science in Industrial Management from Technion-Machon Technologi Le' Israel, completed between 2005 and 2010. Her academic background provided a strong technical and managerial foundation for her career in regulatory affairs and quality assurance.
Regulatory Expertise
Yonit Ringel specializes in leading global regulatory strategies for medical devices. Her areas of expertise include ISO13485 Quality Management Systems, 510(k) submissions, and CE marking processes. Her focus is on achieving efficient and timely clearance of medical devices, ensuring compliance with all regulatory requirements.