Robert Arce has more than 30 years of experience in pharmaceutical manufacturing processes, quality assurance, quality auditing, and GMPs/ GLPs. He is experienced in SOP writing forms, Certificates of Analysis, Testing Certificates, and other controlled documents. His background is in GMP regulated environments including drugs, dietary supplements, cosmetics, packaging, quality assurance, and laboratory systems.
Prior to joining Tampa Bay Analytical Research, Arce worked in Quality Assurance positions at Johnson and Johnson, Smith & Nephew, R. P. Scherer, and JMI-Daniels Pharmaceuticals, Inc.
Arce holds a Bachelor’s degree in Chemistry from Interamerican University of Rio Piedras, P.R. and is bilingual in English and Spanish.
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With the passing of the GMPs and the increasing competitiveness of the dietary supplement market, there is an enhanced focus on product quality.Learn More
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