Scientist I with 4+ years of experience in molecular bioanalytical data for cell and gene therapy
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Detail-driven Scientist I with 4+ years of experience delivering audit-ready molecular bioanalytical data for cell and gene therapy programs in a GLP/GCLP-regulated environment. Proven track record across six-plus GLP-regulated AAV and cell/gene therapy studies, executing high-throughput automated workflows (600-800+ samples per study via KingFisher Flex and QIAcube HT) and validated qPCR, RT-qPCR, and ddPCR assays that have consistently supported successful regulatory audits. Adept at 21 CFR Part 58 method validation (LOD/LOQ, accuracy, precision), root-cause troubleshooting, and translating complex bioanalytical data into clear, actionable results.
A trusted cross-functional partner to Study Directors, QA, and CROs, known for combining strong technical rigor with dependable, on-schedule delivery.
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