Lead bioinformatics scientist with 10+ years in clinical NGS diagnostics within CAP/CLIA/GMP-regulated environments, specializing in pipeline architecture, variant interpretation, and production-scale genomic workflows. …
Lead bioinformatics scientist with 10+ years in clinical NGS diagnostics within CAP/CLIA/GMP-regulated environments, specializing in pipeline architecture, variant interpretation, and production-scale genomic workflows. Delivers up to 40% reduction in analysis turnaround, sustains >98% diagnostic accuracy, maintains 100% audit readiness, and aligns bioinformatics strategy with clinical, quality, and manufacturing operations.
Directed cross-functional operations across 12 staff, increasing execution efficiency by 18% and stabilizing service delivery across core workflows, Deployed AI-enabled inventory system, reducing cost overruns by 25% and improving stock accuracy by 30% across supply operations, Restructured workforce model, eliminating redundancies and reducing labor expenditure by 30% while sustaining operational output, Standardized operational governance frameworks, reducing deviation rates by 22% and strengthening process control adherence across teams, Implemented performance monitoring systems, increasing productivity consistency by 15% through data-driven operational oversight
Architected and scaled NGS pipelines for viral detection across cell bank and bulk harvest programs, supporting 20+ GMP-regulated manufacturing campaigns annually, Accelerated analysis throughput by 40% through optimized pipeline orchestration across AWS and on-premise compute environments, Established ALCOA-aligned data governance frameworks, sustaining 100% audit readiness across regulated bioinformatics workflows, Strengthened collaboration with virology, quality, and manufacturing teams, improving data integration and reducing issue resolution timelines by 30%
Engineered variant interpretation workflows, reducing complex case review time by 35% and improving clinical decision turnaround, Sustained diagnostic accuracy above 98% across high-volume variant review operations within clinical genomics testing, Optimized sequencing workflows from extraction through data generation, increasing end-to-end efficiency by 28%, Resolved bioinformatics and operational constraints, achieving 99% adherence to clinical turnaround time targets across testing programs
Coordinated development operations across multiple programs, increasing on-time execution by 20% within product pipelines, Advanced development of 5+ laboratory-developed tests through structured experimental design and analytical validation workflows, Integrated automation frameworks into laboratory processes, reducing manual workload by 25% and improving reproducibility across assays
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