Mira seeks a Regulatory Submission Specialist to lead regulatory documentation for IVD devices. You will ensure clinical, analytical, usability, risk-management, quality, and labeling evidence is compiled into submission-ready materials and supports compliance across the product lifecycle. The idóneo candidate has experience in regulatory submissions, technical documentation, and international IVD regulatory requirements, with strong writing, project management, and cross-functional coordination
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📌 Remote Regulatory Submission Lead – IVD (Mogán)
🏢 Mira
📍 Mogán
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