John Zenno has over 35 years of experience in the pharmaceutical industry, in medical research, quality assurance, and regulatory affairs. He is currently the head of his own consulting firm, providing expertise in regulatory and quality operations and project management to the industry. His past positions include having been Executive Director of Quality and Regulatory Affairs for a biologics company, and Executive Director of Quality Assurance and Regulatory Compliance for a major contract research organization. He has held positions as Director of Worldwide Regulatory Affairs for a biotechnology company, and Corporate Director of Regulatory Affairs and Quality Assurance for the U.S. Research and Development arm of a major international pharmaceutical corporation. He has extensive experience in regulatory submissions, auditing, training and development, and has authored a book chapter on Orphan Drugs, along with numerous presentations at professional meetings. He has a Bachelor's degree in zoology and physiology from Rutgers and an MS in QA/RA from Temple University.

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