Global Regulatory Affairs Specialist - Software (Hybrid)
Dexcom Inc.
Dexcom Inc. is seeking a Regulatory Affairs Specialist to support development activities for our CGM software products and to develop regulatory strategies for submissions worldwide. You will collaborate with regional teams to align global regulatory plans and ensure labeling and documentation meet international requirements. The role requires strong technical writing, ability to work independently, and experience with 510(k) submissions or EU MDR. #J-18808-Ljbffr Dexcom Inc.
Vacancy posted 1 day ago
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