At GSK, I build LLM workflows for pharmaceutical regulatory-change assessment across eight countries, covering OCR ingestion, evidence retrieval, approval classification, required-document determination, and report generation.
I redesigned a broad LLM task into a four-pass workflow with structured outputs, self-consistency voting, semantic matching, and deterministic policy validation. I also built end-to-end retrieval and achieved 85%+ SME agreement on approval type and required documentation.
Previously, I helped reduce GSK document-generation time by 70%, built FastAPI integrations that cut OCR calls by 50%, and developed scientific-research Q&A capabilities. I’ve also built deep-learning medical-imaging models, published an IEEE TENCON paper, and shipped Python, FastAPI, and MCP projects.

