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Matt Shumway

Matt is a collaborative and results-driven scientist with a broad range of expertise in biotech and pharmaceutical R&D, specializing in Analytical Development and CMC (Chemistry, Manufacturing, and Controls) efforts. His work is rooted in a strong foundation of scientific knowledge and a proven ability to solve complex problems while maintaining focus on timelines and facilitating program development. With a diverse skill set across various analytical techniques, including Mass Spectrometry (MS), Liquid Chromatography (LC), Electrophoresis, Spectrophotometry, and Amino Acid Analyses, Matt brings a unique balance of scientific and quality-driven approaches to my work. He has successfully authored reports for FDA Post-Marketing Commitment submissions and led engineering change management processes, ensuring compliance and efficient product development. With experience in client and vendor management, Matt has supported both early and late-stage programs, managing outsourced analytical tasks across multiple sites. As a skilled collaborator, he works diligently to drive process improvements that enhance reliability, safety, and efficiency within scientific and technical operations.

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