At Acron Aviation, I support the team rebranding products acquired from Honeywell by checking documents for correct fine print, logos, watermarks, and export classifications. I update and manage documents in QMS and ERP systems, edit files, and publish them to the appropriate repositories.
At Formulated Solutions, I edited and formatted SOPs, batch records, stability protocols, and other documentation for a GMP-regulated CDMO. I also sent documents for approval and issued them in accordance with FDA GMP and GDP standards.
My earlier work includes servicing Baxter Spectrum V9 infusion pumps at IQVIA and documenting repairs to FDA GDP standards. I hold a Master of Engineering in Biomedical Engineering from Rowan University and have experience in quality systems, document control, and biomedical equipment.

