Matteo Mussi has extensive experience in laboratory quality control and regulatory affairs within the pharmaceutical industry. Since December 2012, Matteo has served as Responsabile controllo qualità at LabAnalysis, overseeing all quality control documentation and drafting protocols for analytical method transfers in compliance with GMP standards. Prior roles include Tecnico di laboratorio, performing stability analyses on finished pharmaceutical products using HPLC and UV instrumentation, and a temporary position as Responsabile di Area, coordinating laboratory activities. Prior to LabAnalysis, Matteo worked at Teofarma S.r.l. as a Regulatory Affairs Assistant, specializing in regulatory documentation and submissions, and as an Operatore controllo qualità, conducting laboratory analyses on raw materials and finished products. Matteo holds a Laurea Magistrale in Chemistry and a degree in Analytical Chemistry from Università di Pavia.
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