Reuben Lawson
About Reuben Lawson
Reuben Lawson serves as the Vice President of Regulatory Affairs and Quality Systems at Big Health, bringing extensive experience in regulatory affairs for medical devices. His background includes significant roles at Johnson & Johnson and ImpediMed, where he developed expertise in compliance and quality management.
Current Role at Big Health
Reuben Lawson serves as the Vice President of Regulatory Affairs and Quality Systems at Big Health. He has held this position since 2022, contributing to the company's regulatory strategies and quality management systems. His role involves ensuring compliance with applicable regulations and standards, thereby supporting the development and market entry of health products.
Previous Experience at Johnson & Johnson
Reuben Lawson has a substantial history with Johnson & Johnson, where he worked in various roles from 2006 to 2016. His positions included Regulatory Affairs Manager, Senior Regulatory Affairs Manager, and Associate Director of Regulatory Affairs. During his tenure, he focused on regulatory compliance and quality assurance processes across multiple locations, including Irvine, CA, and Minneapolis, MN.
Experience at ImpediMed
Lawson served as the Senior Director of Regulatory Affairs and Clinical at ImpediMed from 2016 to 2022. In this role, he was responsible for overseeing regulatory strategies and clinical operations, ensuring that products met necessary regulatory standards. His work contributed to the advancement of medical devices within the company.
Educational Background
Reuben Lawson studied at The University of Waikato, where he earned multiple degrees between 1993 and 1998. He achieved a Bachelor of Arts with majors in German and History, as well as a Bachelor of Laws. This educational foundation supports his expertise in regulatory affairs and compliance in the medical device industry.
Expertise in Regulatory Compliance
Lawson possesses significant expertise in regulatory compliance, particularly with Class 1 and 2 medical devices. He is knowledgeable about 21 CFR Part 820 and ISO 13485 standards. His experience includes managing recalls and field actions, as well as handling issue escalation and Quality Review Board processes, demonstrating his capability in maintaining product safety and compliance.