Jon Voss
About Jon Voss
Jon Voss serves as the Head of Quality at Abeona Therapeutics in Cleveland, Ohio, a position he has held since 2021. He has extensive experience in quality management within the pharmaceutical industry, having held senior roles at several companies, including Avedro, Genzyme, and Sarepta Therapeutics.
Work at Abeona Therapeutics
Jon Voss has served as the Head of Quality at Abeona Therapeutics since 2021. In this role, he oversees quality assurance and compliance processes, ensuring that the company's operations meet regulatory standards. His leadership contributes to the development and implementation of quality systems that support the company's therapeutic advancements. Abeona Therapeutics is located in Cleveland, Ohio, where Voss has been instrumental in enhancing the organization's quality framework.
Education and Expertise
Jon Voss holds a Bachelor of Science degree in Physiology from the University of California, Davis, which he obtained from 1978 to 1983. He furthered his education at Boston University, earning a Master of Science in Biomedical Engineering from 1984 to 1989. His educational background provides a strong foundation for his expertise in quality management within the pharmaceutical industry, particularly in regulatory compliance and quality system remediation.
Background in Quality Management
Voss has extensive experience in quality management across various organizations in the pharmaceutical sector. He has held significant roles, including Vice President of Quality at Avedro, Inc. and Sarepta Therapeutics, and Executive Vice President of Global Quality at Cellectis. His background includes managing Consent Decree programs, quality system remediation, and regulatory filings, showcasing his proficiency in maintaining compliance and improving quality standards.
Professional Experience in the Pharmaceutical Industry
Throughout his career, Jon Voss has worked in several key positions that highlight his expertise in quality assurance and regulatory compliance. He has held roles at Genzyme, where he served as VP Corporate Quality Systems and VP Operations, and at Amgen as Manager of Validation. His experience spans over three decades, during which he has developed skills in due diligence, acquisition integration, and operational excellence, particularly in LEAN methodologies.
Achievements in Quality Systems
Jon Voss has a proven track record in quality system remediation and operational excellence. His work has involved identifying and correcting deficiencies in quality systems, ensuring that organizations meet rigorous regulatory standards. His expertise in managing quality processes has been critical in various roles, particularly during his time at Genzyme and Cellectis, where he contributed to the development of effective quality management frameworks.