I have hands-on experience in LC-MS/MS method development, validation, and regulatory compliance. I've worked on both Non-GLP and GLP studies with all of my studies passing FDA and regulatory audits. I'm skilled with Sciex and Agilent LC-MS/MS platforms and enjoy collaborating across teams to solve technical challenges and deliver high-quality data. I'm now looking to bring my problem-solving skills and scientific rigor to a new opportunity where I can continue growing and making an impact.