Chiesi Group is seeking a seasoned professional to lead industrialization, validation, and lifecycle management for device components and drug-device combinations. You will drive cross-functional programs across R&D;, Quality, Regulatory, Engineering, and CMOs to ensure robust processes and timely delivery.
Based in Parma with regular travel to sites, you will guide validation activities, risk assessments, and technology transfer while aligning with ISO 13485 and other global regulatory
📌 Senior Device Industrialization (Parma)
🏢 Chiesi Group
📍 Parma
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