Senior Regulatory Specialist - Medical Device Submissions

A medical equipment company is seeking a Mid-Senior level Quality Assurance professional to assist with regulatory documentation and medical writing. The role involves reviewing engineering test reports, monitoring regulatory requirements, and ensuring compliance with FDA regulations. Ideal candidates will have at least 3 years of experience, strong writing skills, and proficiency in Microsoft Office Suite. This full-time position offers a competitive salary ranging from $80,000 to $120,000 annually, based in Minneapolis, Minnesota.
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