Bridging regulated biotech manufacturing with structured data systems, process optimization, and operational workflow design.
Focused on improving clarity, compliance, and efficiency across GMP-regulated environments through systems thinking and automation.
I work at the intersection of cell therapy manufacturing and data systems, supporting regulated biotech environments through structured workflows, documentation optimization, and operational process design.
With a background in Management Information Systems, I bring a systems-thinking approach to manufacturing operations—focusing on improving clarity, traceability, and efficiency across GMP-compliant processes.
My work centers on translating complex operational challenges into structured, repeatable systems that support compliance, cross-functional collaboration, and scalable process improvements.
A full-stack room booking system enabling scheduling, equipment tracking, and administrative management. Built using PHP, MySQL, HTML, and CSS.
Automated data extraction and Excel reporting workflows to improve operational reporting visibility and reduce manual reporting effort.
I contribute to operational improvements by translating complex workflows into structured, repeatable systems. I focus on documentation quality, compliance-oriented thinking, and cross-functional collaboration to improve clarity and consistency.
Email: nyansonbridget@gmail.com
LinkedIn: bridget-nyanson-ayeh