Global Regulatory Affairs Lead - Medical Devices
Global Regulatory Affairs Lead - Medical Devices
Posted yesterday
SENIORITY
Manager
About the role
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
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