Elisabeth Guarch is an experienced professional with a strong background in quality assurance and validation within the pharmaceutical industry. Since October 2018, Elisabeth has served as the Sr. Director of Third Party Quality at Alvogen. Prior roles include Director of QA R&D at Teva Pharmaceuticals from November 2009 to July 2018, and Associate Director of Technical Services at Actavis from November 2007 to October 2009. Elisabeth's experience also encompasses positions as Technical Services Manager at PLIVA, Sr. Validation Specialist at Purdue Pharma, Validation Engineer-Validation Manager at Halsey Drug, Validation Engineer at Alcon Laboratories, Inc., and Microbiologist at Novartis. Elisabeth holds a B.S. in Biology with a focus on Microbiology from Universitat Autònoma de Barcelona, obtained between 1990 and 1994.
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