Orthofix in Bussolengo (VR) seeks a Senior International Regulatory Specialist to lead global regulatory submissions and ensure compliance with EU MDR and US FDA requirements. You will prepare and maintain up-to-date regulatory Product Applications Files, collaborate with Quality, R&D; and Commercial teams, and support inspections and registrations across international markets.
The role is full-time, on-site with a competitive salary package and benefits, offering the chance to work with a
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📌 Global Regulatory Specialist – Medical Devices (Verona)
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📍 Verona
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