Hirdesh Singh has extensive work experience in the pharmaceutical industry, with roles in quality and validation management. Hirdesh started their career in 2002 as a Process Engineer at ADVENT Engineering Services, Inc. In 2004, they joined Amgen as a Senior Engineer. From 2008 to 2010, they worked as a Senior Consultant at Invensys. In 2010, they joined Sanofi Genzyme as a Manager of Quality and Validation. Hirdesh then moved to Alnylam Pharmaceuticals in 2015, where they held various roles including Associate Director, Director, and Sr. Director of Manufacturing Validation. Currently, they are working as an Executive Director of Product Quality at Kymera Therapeutics, starting in 2021.
Hirdesh Singh has a Master's degree in Chemical Engineering from the University of Massachusetts Lowell. Hirdesh also attended the National Insitute of Technology (REC), Jalandhar, but further details about their degree or field of study are not available.
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