About this role
Platform Principal Regulatory Affairs Specialist at Merit. Location: Utah or United States. Role: ensuring compliance, developing strategy, supporting audits Requirements: Bachelor's degree or equivalent experience in a technical field; 15+ years regulatory submissions experience in the medical device industry; expert knowledge of medical device regulations (e.g., ISO 13485, design controls). Category: Legal and Compliance Seniority: Senior Level Commitment: Full Time Workplace: Remote Languages: English