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Carlos Lugo has a diverse and extensive work experience spanning over several companies. Carlos began their career in 1994 as a Manufacturing Supervisor at Baxter International Inc. Carlos then joined Bristol-Myers Squibb in 1995 and held various senior manufacturing, regulatory, and compliance positions until 2004. Carlos then moved to Johnson & Johnson, where they initially worked as a Regulatory Affairs Manager from 2004 to 2008, and later as an Associate Director of Post Market Surveillance from 2008 to 2010.

In 2010, Carlos joined Hospira as the Director of Device Quality Operations until 2012. Carlos then transitioned to Merck, where they served as the Director of Quality and Compliance for Drug Delivery Devices, Vaccines, and Biologics from 2012 to 2014. Carlos then worked at Bayer as the Director of Global Quality Systems & Combination Products from 2014 to 2016.

Carlos is currently employed at Sutro Biopharma, Inc., where they have held various positions. Carlos started as a Senior Director of Quality from 2016 to 2018, then became an Executive Director of Quality & CMC Regulatory Affairs from 2018 to 2020. Currently, Carlos serves in the role of Vice President of Quality & CMC Regulatory Operations since August 2020.

Throughout their career, Carlos has showcased their expertise in quality control, compliance, and regulatory affairs across multiple industries, including pharmaceuticals, biopharmaceuticals, and medical devices.

Carlos Lugo obtained their Bachelor of Science in Chemical Engineering from the Universidad de Puerto Rico during the period of 1989 to 1994.