About this role
Senior Regulatory Affairs Specialist at Meridian Bioscience, Inc.. Location: United States. Role: supporting regulatory, drafting submissions, conducting audits Requirements: Bachelor's in a life science and 4+ years regulatory affairs experience including 510(k), Pre-IDE, EU Technical Files, STED and Canadian licenses; FDA/ISO knowledge, risk management (ISO 14971), and strong project and communication skills. Category: Quality Assurance Seniority: Mid Level Commitment: Full Time Workplace: Remote Languages: English