Rodney Hasler
About Rodney Hasler
Rodney Hasler serves as the Director of Software Quality Assurance at Breg, where he has worked since 2016. He has extensive experience in the medical device industry, having held various leadership roles at companies such as Alaris Medical Systems and CareFusion, and possesses a strong background in regulatory compliance and Human Factors Engineering.
Work at Breg
Rodney Hasler has been employed at Breg since 2012, currently holding the position of Director Quality Engineering. In this role, he has developed and implemented a comprehensive software development process that ensures rigorous oversight of all software validations in both product development and business applications. Additionally, he has served as Director Software Quality Assurance since 2016, focusing on maintaining high standards of quality in software engineering.
Previous Experience in Medical Device Industry
Rodney Hasler has extensive experience in the medical device industry, having worked in various roles across multiple companies. He served as Senior Technical Field Response Manager at Alaris Medical Systems from 2000 to 2002 and held the position of Director, Dispensing Development Quality at CareFusion from 2009 to 2011. His career also includes roles at Cardinal Health, where he was Director of Development Quality Engineering from 2005 to 2009, and Senior Manager of Operations Quality Engineering for 11 months in 2005.
Education and Expertise
Rodney Hasler holds a Bachelor of Science degree in Zoology from Eastern Illinois University, which he attended from 1975 to 1980. He furthered his education at Texas A&M University, earning a Master of Engineering in Bioengineering from 1982 to 1986. He also pursued studies toward a Doctor of Veterinary Medicine (DVM) at the University of Illinois at Urbana-Champaign for a year in 1980. His expertise includes Human Factors Engineering and Risk Management according to ISO 14971 standards.
Regulatory Compliance and Relationships
Rodney Hasler possesses a strategic business approach to regulatory compliance, leveraging his diverse leadership experience in the medical device industry. He is known for building strong relationships with FDA regulators, which enhances regulatory compliance strategies. His extensive background in quality assurance and engineering contributes to improved safety and compliance in medical device development.