Charles River Laboratories
Minnie Davis, MBA, is an accomplished professional with extensive experience in quality assurance and regulatory compliance within the pharmaceutical and biotechnology industries. Currently serving as Associate Director of Quality Systems at Charles River Laboratories since June 2022, Minnie has previously held key roles at Catalent Pharma Solutions, including Interim Director for the Supplier Quality Department and Senior Manager in various quality assurance capacities. Minnie's career also includes significant positions at Emergent BioSolutions and CEL-SCI Corporation, demonstrating expertise in batch release and raw materials quality management. Educational credentials include a Master of Business Administration from Florida Institute of Technology and a Bachelor of Science in Chemistry from Morgan State University.
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Charles River Laboratories
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Charles River Laboratories International, Inc. is an early-stage contract research company. The Company is engaged in laboratory animal medicine and science (research model technologies) and develop a portfolio of discovery and safety assessment services, both good laboratory practice (GLP) and non-GLP, which supports its clients from target identification through non-clinical development. The Company operates in three segments: Research Models and Services (RMS), Discovery and Safety Assessment (DSA), and Manufacturing Support (Manufacturing). The RMS segment includes Research Models and Research Model Services. The DSA segment includes Discovery Services and Safety Assessment. The Manufacturing segment includes Microbial Solutions, Avian, Biologics and Contract Manufacturing. The Company also provides a suite of products and services to support the Company's clients' manufacturing activities.