Steve Johnson
About Steve Johnson
Steve Johnson serves as the Vice President of Quality Assurance and Regulatory Affairs at ECA Medical Instruments, where he oversees global quality assurance and regulatory compliance. He has extensive experience in quality assurance and regulatory affairs, having previously held positions at Abbott Diagnostics and Hycor Biomedical.
Current Role at ECA Medical Instruments
Steve Johnson serves as the Vice President of Quality Assurance and Regulatory Affairs at ECA Medical Instruments. He has held this position since 2017, overseeing global quality assurance, regulatory affairs, validation, and quality control. Johnson reports directly to the CEO and is responsible for ensuring compliance with industry standards and regulations. He also acts as the Management Representative for ECA Medical Instruments' facilities located in Thousand Oaks, CA, and Newbury Park, CA.
Previous Experience at Hycor Biomedical
Prior to his current role, Johnson worked at Hycor Biomedical as the Director of Quality and Regulatory Affairs for one year, from 2010 to 2011. He later served as the Vice President of Operations, Quality, and Regulatory at the same company from 2011 to 2017. His experience at Hycor Biomedical contributed to his expertise in quality assurance and regulatory compliance.
Background in Abbott Diagnostics
Johnson has an extensive background at Abbott Diagnostics, where he worked for a total of 14 years in various roles. His positions included Quality Assurance Management from 2002 to 2010, Manager of Hematology Customer Support from 1998 to 2002, and Technical Operations Management from 1990 to 1998. This experience provided him with a solid foundation in quality assurance and customer support within the diagnostics industry.
Education and Academic Qualifications
Steve Johnson studied at the University of Wisconsin-Stevens Point, where he earned a Bachelor of Science degree in Chemistry. His academic background has supported his career in quality assurance and regulatory affairs, providing him with the necessary technical knowledge to excel in his roles.
Expertise in Quality Assurance and Regulatory Affairs
Johnson possesses a broad background in technical operations, quality assurance, and regulatory affairs. His focus is on compliance and efficiency while meeting customer needs. His extensive experience in the medical instruments and diagnostics sectors has equipped him with the skills to navigate complex regulatory environments and ensure high standards of quality.