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Regulatory Affairs Engineering Lead, Clinical Evaluation

NHNeko Health, Remote

You will own the clinical evaluation strategy and documentation for Neko Health's regulatory submissions to the FDA, EU, and UK, including authoring clinical evaluation plans and reports that support the company's medical device submissions. This requires deep expertise in clinical evidence generation, ISO 14155 clinical investigations, and regulatory documentation, with proven ability to mentor colleagues on regulatory topics.

Posted September 21, 2026 (11d ago)