Job description

Unity Partners exclusively on behalf of our MedTech AI partner

We have been retained by a fast-growing digital health scale-up in their search for a QA Manager with the ambition to grow into Head of Quality. This company develops an AI-powered CE-marked medical device with a global user base. Quality and compliance are not an afterthought here — they are built into the product from day one.

The role comes with a clear growth trajectory: within roughly a year, the expectation is that you take full independent ownership of the Quality function.

Role Overview

As QA Manager you are responsible for the QMS and act as the go-to person on all quality and compliance topics. This is a SaMD environment, which means your work covers not just classic medical device quality but also software lifecycle management, algorithm quality, cybersecurity and data privacy.

Key Responsibilities

  • Keep the QMS fit for purpose and audit-ready across EU MDR, MDSAP and FDA frameworks
  • Run internal and external audits, drive CAPA resolution and keep complaint handling on track
  • Manage document control, training compliance, supplier oversight and management reviews
  • Apply relevant software and risk standards (ISO 14971, IEC 62304, IEC 62366) across design controls and V&V
  • Maintain the ISMS and ensure ongoing compliance with ISO 27001, NEN 7510 and GDPR
  • Keep technical documentation, product release and post-market surveillance in good shape
  • Work closely with Regulatory, Product, Clinical and Operations to make quality part of how the business operates
  • Play a key role in the transition from the current QMS setup toward a future eQMS

Your Profile

  • 7+ years in medical device QA, with a strong preference for SaMD or digital health backgrounds
  • Familiarity with AI/ML in a regulated context is a real plus
  • Experience guiding or implementing a QMS-to-eQMS transition is a clear advantage
  • Comfortable growing into a team lead role within about a year
  • Solid working knowledge of ISO 13485, EU MDR, MDSAP, FDA 21 CFR Part 820, and the relevant software standards
  • Experience with information security compliance and GDPR in practice
  • You build structure without slowing things down
  • Fluent in English; Dutch is a strong plus
  • Amsterdam-based; hybrid working with regular on-site presence required

Why join?

  • A role with real ownership and a genuine path to Head of Quality
  • Direct impact on a product that improves early detection of serious disease
  • Informal, international team with short lines and genuine ambition
  • Hybrid working from Amsterdam, competitive salary, 25 holidays and development budget

Interested?Let's connect. Unity Partners is exclusively supporting this confidential search.christian@unitypartners.nl | +31 (0)20 8938 606

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