Jason Easley
About Jason Easley
Jason Easley is a Manager of Regulatory Affairs and Quality Assurance at Pursuant Health, with a background in quality systems and regulatory compliance. He has over 15 years of experience in the field, having held various quality-related positions in several medical organizations.
Current Role at Pursuant Health
Jason Easley serves as the Manager of Regulatory Affairs and Quality Assurance at Pursuant Health. He has held this position since 2018, contributing to the organization's commitment to maintaining high standards in regulatory compliance and quality assurance. His role involves overseeing various quality systems and regulatory elements, ensuring adherence to industry standards and regulations.
Previous Experience in Quality Assurance
Before joining Pursuant Health, Jason Easley worked at Chemence Medical Products as the Quality Systems Manager from 2014 to 2018. He also served as a Quality Assurance Specialist at Cryolife, Inc. from 2005 to 2008. His experience includes a four-year tenure as a Quality Specialist at the Georgia Eye Bank from 2008 to 2012. These roles have equipped him with a comprehensive understanding of quality systems in the medical field.
Education and Certifications
Jason Easley earned a Bachelor of Science degree in Biology from Oglethorpe University, where he studied from 1995 to 2003. He holds certifications as a Quality Auditor and a Quality Improvement Associate from the American Society of Quality. Additionally, he was previously certified as a Tissue Bank Specialist by the American Association of Tissue Banks.
Expertise in Quality Systems and Regulatory Compliance
Jason Easley possesses extensive experience in building and improving quality systems and regulatory elements. His expertise includes internal audits, CAPA (Corrective and Preventive Actions), complaints management, process controls, risk management, and document control. He has established key Quality System subsystems and enhanced compliance with regulatory guidelines, including Title 21 CFR 820, ISO 13485:2003, and MDD 93/42/EEC.