Global Regulatory Affairs Lead - Medical Devices

BD in the United States seeks a Regulatory Affairs professional to lead regulatory submissions for medical devices across the US, Europe, and other markets. You will develop regulatory strategies and manage submissions to ensure lifecycle compliance across V&V, risk management, usability, reprocessing, and software development. You will collaborate with R&D, Quality, Manufacturing and Marketing to align product development with regulatory requirements and business goals, writing SOPs and #J-18808-Ljbffr

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Vacancy posted 12 hours ago

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