Senior Regulatory Program Lead, Medical Devices
Johnson & Johnson MedTech
Johnson & Johnson MedTech in Plymouth, MN seeks a Sr Program Lead, Regulatory Affairs to lead global regulatory strategies for medical devices and ensure timely commercialization in compliance with FDA and worldwide regulations. The role requires a Bachelor's degree in engineering or sciences and 5+ years in regulatory affairs for medical devices, with strong negotiation and project management skills and collaboration across cross-functional teams. #J-18808-Ljbffr Johnson & Johnson MedTech
Vacancy posted 1 day ago
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