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Carlos D. Rivera-Adrovet is a seasoned Quality Assurance professional with 20 years of combined experience in the pharmaceutical industry, evenly split between commercial and R&D supporting Quality Management Systems governing global clinical trials and national/international Active Pharmaceutical Ingredients and Drug Product manufacturing.

He has spent the last decade implementing and supporting Quality Management Systems in several pharmaceutical organizations that had led companies to successful regulatory inspections, mergers, and acquisitions.

Previously, Carlos was the Head of the Quality Department at NiKang Therapeutics and Peloton Therapeutics. He also held several quality roles at Merck, Cempra, Pfizer, BMS, Abbott and Wyeth.

Carlos received his undergraduate degree in microbiology from University of Puerto Rico Humacao in 2001. He is certified by the American Society of Quality as Quality Auditor and Pharmaceutical GMP Professional.