Global Regulatory Affairs Lead - Medical Devices
Abbott
Abbott is seeking a Principal Regulatory Affairs Specialist for its Vascular Division, on-site in Santa Clara, CA or Temecula, CA. You will lead regulatory strategies for endovascular devices, manage global submissions, and partner with Regulatory, Quality, Clinical, R&D, Manufacturing and others to ensure lifecycle regulatory compliance. The role requires extensive knowledge of US/EU regulatory pathways, 510(k)/PMA submissions and EU MDR, with opportunity to mentor junior colleagues and drive #J-18808-Ljbffr
Vacancy posted 2 days ago
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