Director, Global Manufacturing & Regulatory Affairs

A leading medical device company in the Town of Florida seeks a Director of Manufacturing & Regulatory Affairs to lead and scale manufacturing and regulatory operations. This role requires 8–15+ years of experience in medical device or regulated skincare manufacturing, expertise in ISO 13485 compliance, and a strong understanding of quality management systems. The successful candidate will have hands-on experience with ISO-certified environments and a proven track record in regulatory submissions. This position offers competitive salary and growth opportunities.
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