Ceva
Alicia Henk serves as the Director of Pharmaceutical Regulatory & Development at CEVA SANTE ANIMALE since August 2012, overseeing CMC development, registration, manufacturing, and scale-up for veterinary pharmaceutical drug products. Prior to this role, Alicia held the position of CMC Manager in Pharmaceutical Development & Regulatory Affairs at CEVA SANTE ANIMALE from January 2008 to 2012. Alicia's extensive experience includes over a decade at Pfizer as Sr Manager of Technical Support, where responsibilities encompassed product development, scale-up, transfer, CMC regulatory submissions, and validation. Alicia holds a Bachelor of Science degree in Life Sciences from the University of Nebraska-Lincoln and completed an Advanced Certification in Regulatory Affairs from San Diego State University in 2009.
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