Senior Regulatory Affairs Lead, Vascular Devices
Abbott Laboratories
Abbott Laboratories is seeking a Principal Regulatory Affairs Specialist for the Vascular division, working on-site in Santa Clara, CA or Temecula, CA. You will lead regulatory strategy, manage global submissions (FDA, EU MDR), and support product lifecycle from development through commercialization. The role requires 6–8 years in medical devices, experience with Class II/III devices, and strong collaboration across functions. Base pay ranges widely, with opportunities in a matrixed environment. #J-18808-Ljbffr Abbott Laboratories
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