Descrizione del lavoro
Who we are looking forPurposeAccountable for:• Pursuing and executing global, robust and innovative Regulatory-CMC strategies, across the entire life-cycle (pre-clinical, clinical, life-cycle and change management) of Chiesi global products and projects, intended as chemically synthetized or biologics DS, DP, medical devices (including the device component of combination products).• Acting as GRA representative or leader for CMC topics in the project teams to ensure proper planning and communication as well as to support decision-making. • Writing of Internal Reg CMC WI/SOP, revision or contribution...