About this role
Principal Regulatory Affairs Specialist – Diabetes Care (on-site) at Abbott. Location: Alameda, California, United States. Role: leading submissions, developing strategy, ensuring compliance Requirements: Bachelor's in scientific discipline; experience with IVD/medical device regulatory submissions, 21 CFR 820, ISO 13485 and EU MDR/IVDR; RAC a plus; ability to develop strategy, lead submissions, and interact with agencies. Category: Legal and Compliance Seniority: Senior Level Commitment: Full Time Workplace: Onsite Languages: English