Deborah Smith

Deborah Smith is a retired professional with a wealth of expertise in Quality, GMP, Analytical Development, and the establishment of Quality Systems. She has a strong background in managing manufacturing facilities and laboratories, implementing continuous improvement initiatives, and ensuring harmonization of SOPs.

With a solid educational foundation including a Bachelor's degree in Chemistry from Duke University and a Ph.D. in Chemistry from the University of Virginia, Deborah has honed her skills over the years to become a respected leader in her field.

Throughout her career, she held key positions at reputable organizations such as GSK and Novartis, where she served as the Quality Systems Lead (Global Head), Head of Quality Systems & Standards for OTC, Executive Director of the Clinical Manufacturing Unit, and Associate Director of Analytical R&D among others.

Deborah has been instrumental in preparing organizations for audits and inspections, leading global projects, and excelling in technical project management. Her ability to thrive in a global, multicultural, and matrixed environment has been a significant asset to the companies she has worked for.

Her areas of specialization encompass OTC products, Brand Pharmaceuticals, and Generics. Deborah's extensive experience and knowledge make her a seasoned professional in the pharmaceutical industry, particularly in the realms of quality assurance, regulatory compliance, and operational excellence.