Global Quality Manager

Quality Manager - Global Opportunity to build team and implement QMSEstablished fast-growing Med-tech BusinessMust have experience with Hardware and SoftwareRelocation SupportedMedical Device/ IVD Background essentialAre you ready to take on a role that will shape the quality foundation of one of the fastest-growing diagnostics companies in the world? Have you worked in the European medical device/ IVD market and would be interested in living in Dubai?A pioneering health-tech business is looking for a bright, capable Quality Manager to join its expanding team in Dubai. The company’s innovative diagnostic products are already among the top-selling home diagnostic tests in the US, and they’re now entering a major global growth phase — launching new technologies and preparing for scale across multiple international markets.This role isn’t about maintaining an existing system — it’s about building one for the future. You’ll be responsible for strengthening and scaling a global Quality Management System covering assay, hardware, software, and data science teams. From ISO 13485 implementation to audit readiness and supplier quality, you’ll be the link between innovation and compliance — ensuring the business continues to deliver reliable, life-changing products at pace.You’ll work closely with an exceptional leadership team, in a culture that values intelligence, curiosity, and collaboration.Based in Dubai, you’ll enjoy a world-class lifestyle and a central role in a truly global business.The opportunity:Build a global QMS across next-generation diagnostic technologiesWork in a high-growth, innovation-driven environmentAttractive tax-free salary, performance bonus, and relocation supportLong-term career growth as the business scales internationallyWhat are we looking for: - Skilled leader with 10 years of experience in the medical device or IVD marketDynamic individual capable of working in fast growing business (not a 9-5)Implementer - Built and scaled ISO 13485 QMS; passed CE/FDA/MDSAP auditsMust have experience with Software and Hardware- medical devicesDepth in one or more areas (QMS, Regulatory, Assay, Software, AI/ML) and ability to lead across othersFamiliar with ISO 14971, IEC 62304, IVDR, and global regulatory frameworks (e.g., FDA Class II, IVDR, MDSAP)If you’re excited by the idea of creating impact on a global scale — apply now.