I am a results-driven professional with over 5 years of experience in pharmaceutical manufacturing, quality assurance, and process improvement. I have a proven track record in GMP/GxP compliance, CAPA management, root cause analysis, and operational excellence initiatives, driving efficiency while maintaining regulatory standards.
In addition, I am skilled in data annotation, AI support tasks, and digital workflow management, with strong attention to detail, analytical thinking, and the ability to deliver accurate and timely results. I thrive in cross-functional environments and am passionate about optimizing processes and supporting projects that rely on precision and quality.
I am looking to contribute my expertise to freelance projects that require meticulous attention to detail, process improvement insights, or AI/data-related tasks, delivering high-quality outcomes for clients.