xiaoxuan guo

I’m a pharmaceutical quality professional with 9 years of experience in pharmaceutical and traditional Chinese medicine quality control, GMP-compliant laboratory operations, analytical testing, documentation management, and quality system processes. I focus on SOP lifecycle management, deviation/OOS support, analytical method verification, and quality documentation review, while maintaining document accuracy, traceability, and version consistency under GMP requirements.

I’ve supported CAPA and audit readiness through careful laboratory documentation and confidential, compliance-driven work. Alongside my QA background, I have a strong interest in artificial intelligence applications in life sciences, where I independently explored AI-assisted solutions for pharmaceutical quality management—especially documentation workflow optimization, knowledge management, and SOP information retrieval—while prioritizing regulatory compliance, data integrity, and human oversight.