Scott Stratton
Process Development Scientist Ii at Biobridge Global
Based in San Antonio, United States
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Seniority
Staff
Department
Science
Location
San Antonio
Industry
Biotechnology
Company size
448
Contact information
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s•••••••@biobridgeglobal.org
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Background
About Scott Stratton
PhD-level scientist with GMP-compliant biologics and ATMP manufacturing experience, specializing in process development, tech transfer, and analytical assay validation. Proven track record leading GMP cleanroom readiness, process validation, process performance qualification (PPQ), and regulatory alignment (EU GMP Annex 1, ICH Q8/Q9/Q10). Skilled in scale-up/out, process monitoring, batch release, SOP authoring, change control, deviation investigation, and CAPA. Technical expertise spans mammalian cell culture, bioreactors, aseptic processing, ELISA, qPCR, flow cytometry, and single-use systems alongside analytical development. Client-facing experience in a CDMO environment, delivering process improvements and tech transfer strategies, working alongside manufacturing sciences (MSAT) and operations teams. Published in 10+ peer-reviewed journals with research in regenerative medicine, biomaterials, and cell therapy. Full publication list available on Google Scholar: & hl=en
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