Denise Miller

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Lyophilization Technology
Quality Assurance Associate
Denise Miller began her career with the company in 2008. In 2014, Denise joined the Quality Assurance Group as a Document Control Specialist and was promoted to Quality Assurance Associate in 2018. She is currently responsible for oversight and administration of Quality Systems for the Development Sciences and Clinical Manufacturing. Denise has published and presented poster presentations at focused industry events. She is a member of the American Society of Quality. Denise’s focus is on ensuring clients receive the highest quality and safe lyophilized drug products for their patients.