Jacob Lichtman

Jacob Lichtman is an experienced professional in the pharmaceutical industry, currently serving as a Submission Ready Standards Specialist - CMC at Takeda since November 2022. Prior to this role, Jacob worked as a Document Specialist - Quality Systems/Documentation Control at Sage Therapeutics from March 2022 to October 2022, and held various positions at Takeda, including Nonclinical Regulatory Submissions Documentation Specialist and US Transparency Data Validation Specialist between June 2019 and December 2021. Jacob's career began at Shire as a Transparency Specialist - Data, Process and Controls, and MDM Data Analyst from February 2017 to June 2019, and at Takeda Pharmaceuticals as a Documentation Associate and Intern from May 2015 to February 2017. Jacob holds a Bachelor’s Degree in Geography from the University of Connecticut, obtained in 2015.