About this role
Senior Regulatory Affairs Specialist-Hybrid Fort Lauderdale, FL at Trividia Health, Inc.. Location: Fort Lauderdale, Florida, United States. Role: supporting compliance, conducting assessments, preparing submissions Requirements: B.S. in life sciences/engineering plus 5+ years regulatory affairs experience in medical device/IVD; post-market compliance, change management, and FDA submission exposure; strong technical writing and communication. Category: Legal and Compliance Seniority: Senior Level Tools: Microsoft Office, electronic document management systems Certifications: rac Commitment: Full Time Workplace: Hybrid Languages: English