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Sarah Mae Greene has a diverse work experience in the quality and regulatory compliance field. Sarah Mae started their career as a Quality Systems Specialist at Thermogenesis in 2005 and worked there until 2011. After that, they gained experience as a Document Control Administrator at Specialty Silicone Fabricators from 2012 to 2016. Sarah Mae then worked as a Compliance Analyst at the California Department of Transportation in 2016, followed by a role as a Quality Systems / Document Control Manager at LC Therapeutics, Inc. in 2017. In late 2017, they joined Cesca Therapeutics Inc. as a Quality and Regulatory Compliance Specialist until the end of 2018. Currently, they are serving as a Quality Director at Precision Medical Products since 2019.

Sarah Mae Greene earned a Bachelor of Science (B.S.) degree in Business Management from the University of Phoenix from 2008 to 2010. In 2014 to 2016, they completed a Certificate Program in Medical Product Development from the University of California, Irvine Division of Continuing Education. Sarah Mae also obtained the ISO 13485 Internal Auditor certification from ASQ in 2008.