Global Medical Device Regulatory Specialist (Contract)
Intellectt Inc
A forward-thinking company is seeking a Regulatory Affairs Specialist with a strong focus on compliance and detail. In this exciting role, you will prepare and submit global regulatory filings, ensuring adherence to FDA, EU MDR, and ISO 13485 standards. You will collaborate with cross-functional teams to support product development and regulatory inspections. This position offers the opportunity to make a significant impact in the medical devices sector, working within a dynamic team dedicated to innovation and excellence. If you are proactive and passionate about regulatory affairs, this is the perfect opportunity for you. #J-18808-Ljbffr Intellectt Inc
Vacancy posted 2 days ago
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