More About Me

I am a biomedical engineer with a strong focus on quality, process improvement, reliability, and validation. Through hands-on experience at Mayo Clinic and in academic research environments, I have developed a solid foundation in regulated product development, data-driven decision making, and cross-functional collaboration.

My work has included executing validation protocols such as IQ, OQ, and PQ, leading CAPA investigations, conducting internal quality audits, and applying risk assessment tools like FMEA. I have contributed to maintaining Design History Files, improving testing processes using Minitab, and ensuring compliance with FDA 21 CFR 820 and ISO 13485 standards.

I have also worked on segmentation and simulation workflows using Mimics and 3-matic to process patient-specific anatomical models. I performed stress-strain analyses in ANSYS to support implant validation and design improvements. My research background has strengthened my programming and data analysis skills in R and Python, which I have used for statistical modeling and data interpretation.

Outside of engineering, I enjoy painting with watercolors and acrylics, journaling, and discovering new coffee shops. These creative outlets help me stay grounded and bring a fresh perspective to the work I do.

I strive to bring both precision and curiosity to every project by combining technical excellence with clear communication and a continuous improvement mindset.

My Interests and Hobbies