Regulatory Affairs Specialist – Medical Devices
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Nipro Europe Group Companies, based at the Mechelen, Belgium headquarters, is seeking a hands-on Regulatory Affairs Specialist for the RAQACA team. You will manage regulatory activities for medical devices and IVDs across Europe, Africa, India, and the Americas, coordinating registrations and lifecycle management with internal and external stakeholders.
The role emphasizes collaboration, regulatory intelligence, and process improvement to ensure timely authorizations and continued compliance.