Dorothee Alatorre

Dorothee Alatorre

Associate Director, Regulatory Affairs @ BeiGene

About Dorothee Alatorre

Dorothee Alatorre is the Associate Director of Regulatory Affairs at BeiGene in Emeryville, California, with extensive experience in the biotechnology and pharmaceutical industries.

Current Role at BeiGene

Dorothee Alatorre is currently serving as the Associate Director of Regulatory Affairs at BeiGene in Emeryville, California, United States. This role includes oversight and management of regulatory processes, ensuring that the company's biopharmaceutical products meet all necessary standards and requirements for market approval.

Previous Positions at BeiGene

Dorothee Alatorre has held multiple positions of increasing responsibility at BeiGene. She started as a Regulatory Affairs Manager in San Mateo, California, from 2016 to 2017. She then became a Senior Manager of Regulatory Affairs from 2017 to 2019 in Emeryville, California, before being promoted to her current position. Her experience at BeiGene has been marked by a consistent progression in her career.

Experience at Medivation

Prior to joining BeiGene, Dorothee Alatorre worked at Medivation. She held the position of Regulatory Affairs Associate from 2015 to 2016 in San Francisco, California. Following this role, she was promoted to Senior Regulatory Affairs Associate in 2016, where she served for eight months. At Medivation, Alatorre gained substantial experience in regulatory affairs within the pharmaceutical industry.

Academic Background

Dorothee Alatorre has a strong academic background in science and regulatory affairs. She earned a Ph.D. from Heidelberg University, where she studied from 2001 to 2007. Additionally, she holds a Master's degree from Technische Universität Berlin, completed between 1994 and 2000. She also briefly studied at San Francisco State University in 2013.

Postdoctoral Research Experience

Dorothee Alatorre has significant postdoctoral research experience. She worked at UCSF as a postdoctoral researcher from 2008 to 2009 before moving to the Gladstone Institutes, where she continued her research from 2009 to 2013. This research experience has provided her with a solid foundation in the scientific aspects of regulatory affairs.

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