Leonardo Milioni

I am working on the design and synthesis of HDAC 1/6 inhibitors for Retinitis Pigmentosaand KDM4a inhibitors for leukemia. This involve conducting literature reviews to identify knowledge gaps and guide research directions, including writing scientific reviews. I also collaborate with interdisciplinary teams to conduct studies and generate insights.

During my tenure, I played a key role in the validation and calibration of pharmaceutical machinery, meticulously ensuring compliance with GMP standards. Additionally, I actively participated in the design and drafting of qualification protocols, including PQ, IOQ, and DQ, and contributed to the creation of critical documents such as VP and FRA. I personally managed FATs, acting as a liaison between suppliers and clients. My close collaboration with major clients such as GSK, Philogen, MMI, and Merck Seronocontributed to the development of strong working relationships.

During my thesis internship, titled "Synthesis and PhotostabilityStudies of Morita-Baylis-Hillman Derivatives," I focused on synthesizing compounds specifically designed as fluorescent probes for protein labeling. Throughout this experience, I honed my laboratory skills, including NMR spectroscopy, mass spectrometry, chromatography, and UV-Vis spectroscopy.

Thanks to my role as a pharmacist, I have acquired key skills including prescription management, preparation of compounded medications, and conducting diagnostic tests in the pharmacy. I have managed sensitive documents with a focus on privacy compliance and a customer-centric approach to ensure complete satisfaction. I have consistently collaborated with colleagues in task management.