Ron Stellon is Senior Director of Quality Assurance at AstraZeneca Pharmaceuticals. Previously he was Executive Director of Quality Assurance for Bristol-Myers Squibb and was responsible for GLP, GCP and GMP quality assurance and compliance programs in support of the R&D Division and for GMP quality assurance and compliance for commercial operations in Puerto Rico. He joined DuPont Pharmaceuticals in 1989 as Quality Assurance Manager and has held positions of increasing management responsibility in regulatory compliance and quality assurance. Mr. Stellon strted his career in 1978 with the FDA as an investigator in the Philadelphia District Office, specializing in pharmaceutical and medical device inspections, including sterile products. At FDA, he served as an Acting Supervisor, Recall Coordinator, and Compliance Officer.
Mr. Stellon has a MS in Quality Engineering from Lehigh. He is a member of the PDA, ISPE, and ASQ and is an ASQ certified Quality Auditor and Quality Engineer. He is on the faculty of the PDA Training and Research Institute. He has presented at numerous industry and professional meetings and has published papers related to quality assurance and regulatory compliance activities.

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