MedTech Regulatory Affairs & Quality Leader

A medical technology company in Minneapolis seeks a Vice President of Regulatory Affairs & Quality Assurance to develop global regulatory strategy and ensure compliance with quality standards. This executive role involves leading regulatory submissions and liaising with the FDA and other authorities. The ideal candidate will have over 12 years of experience in regulatory affairs within the medical device sector and a strong understanding of regulatory frameworks. Excellent leadership abilities and a focus on patient outcomes are essential.
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