Becky Hudson
About Becky Hudson
Becky Hudson serves as the Vice President of Regulatory Affairs and Quality Assurance at Maxtec and Perma Pure LLC, having transitioned into the medical device industry after an 11-year career in the Coast Guard. She has held various leadership roles in regulatory and quality assurance across multiple companies, demonstrating a commitment to ethical practices in her field.
Current Role at Maxtec
Becky Hudson currently serves as the Vice President of Regulatory Affairs and Quality Assurance (RA/QA) at Maxtec. She has held this position since 2023, contributing to the company's commitment to regulatory compliance and quality management in the medical device sector. Her role involves overseeing the regulatory processes and ensuring that products meet the necessary quality standards.
Previous Experience in Regulatory Affairs
Prior to her role at Maxtec, Becky Hudson worked as the Director of RA/QA at Alliance Pharmaceuticals Limited for five months in 2023. She also held the position of Director of Regulatory Affairs and Quality Assurance at Alliant Healthcare Products & Surge Cardiovascular from 2010 to 2016. Her extensive experience in regulatory affairs has equipped her with the skills necessary to navigate complex regulatory environments.
Military Background and Transition to Medical Devices
Becky Hudson served as a Coast Guard Veteran for 11 years before transitioning to the medical device industry. Her military background has provided her with a strong foundation in leadership and operational management, which she has applied to her subsequent roles in regulatory affairs and quality assurance.
Educational Background in Electrical Engineering
Becky Hudson studied at the US Coast Guard Academy, where she earned a Bachelor of Science degree in Electrical Engineering from 1994 to 1998. This educational background has contributed to her analytical skills and technical understanding, which are essential in her roles within the medical device industry.
Career in Quality Assurance and Operations
Becky Hudson has a comprehensive background in quality assurance and operations management. She worked as a Quality Engineer/Regulatory Analyst at Stryker Instruments from 2005 to 2008 and served as the Director of Operations at SunTech Medical from 2018 to 2023. Her diverse experience spans various aspects of the medical device field, emphasizing her commitment to quality and regulatory compliance.