Claudia Corredor
Senior Principal Scientist @Bristol Myers Squibb
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WORK HISTORY
Senior Principal Scientist @Bristol Myers Squibb
New Brunswick, NJ, US
Matrix Lead, Oral Solid Dosage (OSD) Formulation & Process DevelopmentMatrix lead for OSD formulation and manufacturing process development, supporting programs from First-in-Human (FIH) through Phases 1–3 and commercial manufacturing. Enabled 15+ assets across 35+ global clinical studies through scalable Engineering Technologies (ET) capabilities.Strategic technical authority for formulation and process optimization, including excipient compatibility, glidant and antioxidant selection, and mitigation of scale-up risk across roller compaction, high-shear wet granulation, tablet compression, encapsulation, and direct compression.Drives accelerated development and robust drug product design by integrating material characterization, multivariate statistics, mechanistic and empirical models, Process Analytical Technology (PAT), automation, and digital engineering.Engineering Technologies representative on cross-functional CMC teams for four portfolio assets (neuroscience, oncology, hematology; Phases 1–2), accountable for defining and executing integrated engineering strategies across Analytical, Biopharmaceutics, Devices, Materials, and Formulation functions.Matrix lead for global technology transfer, ensuring successful transfer of processes and analytical methods across manufacturing sites in the U.S, India, U.K, and Canada, aligning early development intent with commercial readiness.Leads technology transfer and deployment of PAT methods, including inline tablet analysis, NIR, and Transmission Raman, enabling enhanced process understanding and control.Influences product development decisions by applying models, data analytics, and PAT across unit operations (blending, roller compaction, fluid-bed drying, tablet compression, encapsulation), establishing strong linkages between process parameters and drug product CQAs.
EDUCATION
Universidad Nacional de Colombia
B. S. Pharmacy, Pharmaceutical Sciences
University of Central Florida
Ph. D., Chemistry with track on Materials Science
University of Central Florida
M. Sc., Industrial Chemistry
ABOUT CLAUDIA CORREDOR
I am passionate about formulation and process development of oral solid dosage forms (OSD) and Parentals. Broad understanding of the issues in roller compaction, high-shear wet granulation, fluid-bed drying, tableting, and coating and how to solve them. I combine hands-on manufacturing process expertise with strong material science and powder characterization capabilities to design, optimize, and scale robust drug products.My technical background includes critical material attribute testing—including flow, cohesivity, compressibility, compactability, tabletability, ribbon characterization, segregation risk assessment, and particle size characterization—and understanding their relationship to process parameters and unit operations. I routinely apply off-line material characterization techniques in combination with inline process analytical technology (PAT) tools and process data to support process understanding, scale-up, and control strategy development.I work across drug product development and GMP manufacturing environments, leading technology transfer, process scale-up, and commercialization readiness activities. I am experienced in translating complex experimental and process data into clear, science-based decisions that de-risk scale-up, improve robustness, and accelerate development timelines.I am known for connecting formulation science, process modeling, PAT, advanced process control (APC), and digital engineering strategies with program needs. I collaborate extensively across Drug Product Development, Integrated Technologies & Engineering, Manufacturing Science & Technology (MS & T), Material Science & Engineering, and with external partners and CMOs to strengthen technical workflows and enable high-quality execution from early development through commercial manufacturing.I am passionate about solving complex technical problems, elevating formulation and manufacturing capabilities, and delivering practical, well-engineered solutions that move medicines efficiently and reliably to patients.
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