MedTech QA & Regulatory Affairs Specialist - Startup
Pangaea Data Limited
Pangaea Data Limited is seeking a Quality Assurance & Regulatory Affairs Specialist to own the day-to-day QMS operations and drive continuous improvement as the company scales. You will lead ISO 13485 compliance, CAPA, internal audits, and regulatory submissions (CE/MDR, IEC 62304), partnering with engineering, clinical, and leadership teams. This is a hands-on role in a fast-growing MedTech startup with strong mentorship and opportunities to shape regulatory strategy. #J-18808-Ljbffr Pangaea Data Limited
Vacancy posted 2 days ago
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