Global Quality Manager

Overview

Opportunity to build team and implement QMS

• Established fast-growing Med-tech Business
• New role - hands-on building a team
• Must have experience with Hardware and Software medical device
• Medical Device/ IVD Background essential

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.

• Build a global QMS across next-generation diagnostic technologies
• Solve real problems – Dive into assay results, firmware logs, and app data to debug issues and uncover root causes, bringing a first-principles mindset to every quality challenge.
• Ensure accuracy – Define and monitor metrics like limit of detection (LOD), true/false positive rates, and overall diagnostic accuracy to ensure our tests are reliable.
• Lead releases with confidence – Own the go/no-go decision for product releases, ensuring every requirement has traceability and every risk is mitigated so we launch safely and swiftly.
• Work in a high-growth, innovation-driven environment
• Attractive tax-free salary
  , performance bonus
  , and relocation support
• Long-term career growth as the business scales internationally

• Skilled leader with 10 years of experience in the medical device or IVD market
• Dynamic individual capable of working in fast growing business (not a 9-5)
• Implementer - Built and scaled ISO 13485 QMS; passed CE/FDA/MDSAP audits
• Must have experience with Software and Hardware- medical devices - demonstrable experience in ensuring accuracy (E.g. LOD)
• Depth in one or more areas (QMS, Regulatory, Assay, Software, AI/ML) and ability to lead across others
• Familiar 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.