Mira is seeking a Regulatory Submission Specialist to lead and support the documentation required for in vitro diagnostic devices. You will ensure regulatory compliance across submissions and maintain evidence of analytical and clinical performance.
The role involves coordinating with internal teams, external consultants, and regulators to prepare, review, and finalize submission dossiers. This is a remote position offering versátil hours and growth opportunities.
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📌 Remote regulatory submissions specialist — eu ivdr/ce-mark (Cataluña)
🏢 Mira
📍 Cataluña
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