Lee A. Remon

Lee A. Remon has extensive work experience in the pharmaceutical industry. From 2021 to present, Remon has served as a Senior Manager of QA Operations at Sage Therapeutics. Prior to this role, from 2019 to 2021, Remon worked as a Senior Regulatory Project Manager at Paragon BioTeck, Inc., where they managed international contract vendors and prepared registration documentation.

Before joining Paragon BioTeck, Inc., Remon held the position of Global Corporate Quality Manager at Syneos Health Clinical Solutions from 2014 to 2019. In this role, Remon oversaw QA, Compliance, Audit, Trending, and Process Improvement for a global contract research organization, handling quality issues across all stages of drug development.

From 2012 to 2013, Remon worked as a Quality/Compliance Consultant for their own company. Prior to that, from 2011 to 2012, Remon was the Director of Quality Assurance at CoreRx, Inc., where they established and improved quality systems and oversaw compliance during facility construction.

Remon has also worked at Catalent Pharma Solutions from 2001 to 2010, holding roles such as Sr. QA Technical Specialist/Project Manager, Corporate Technical Project Manager-Global, and Sr. QA Technical Review Specialist. At Catalent, Remon provided project management, reviewed technical documentation, and ensured facility compliance with cGMP requirements.

Earlier in their career, Remon worked as a Technical Services Specialist at UDL Laboratories, Inc. from 1997 to 1999, where they managed equipment moves and facility construction projects. Remon also had various student positions as a Medical Assistant from 1990 to 1995.

Overall, Remon's work experience demonstrates a strong background in quality assurance, regulatory affairs, and project management within the pharmaceutical industry.

Lee A. Remon attended the University of South Florida from 1987 to 1995. During this time, they pursued a Bachelor of Science degree in Life Science with an emphasis on molecular genetics.