Sr. QA Engineer
unitypartners.nl·ICT & data·Hbo·nog niet gecontroleerd
Vacaturetekst
Sr. QA Engineer - Unity Partners - Vacatures
Unity Partners exclusively on behalf of our MedTech partner
Our partner is an established player in the medical device industry, developing innovative treatment solutions used by healthcare providers worldwide. With a dedicated focus on a specific product line within their broader portfolio, quality and regulatory compliance sit at the core of how they operate.
To strengthen their Quality team on a structural basis, we are looking for an experienced QA Engineer who can quickly operate independently and make a direct impact from day one.
As QA Engineer, you join a close-knit QA team, working closely alongside the RA team. These teams collaborate cross-functionally with Engineering, Sales & Marketing, Supply Chain and Manufacturing to keep products and processes aligned with current standards and regulations across the medical device industry. This is a permanent position.
Ensure product compliance for an assigned value stream within the product portfolio
Support the local and global QMS and related processes
Represent the QA organisation in processes such as non-conformances, CAPA, and complaint handling, or provide technical input to functions like Order Fulfilment and Manufacturing
Ensure accurate reporting and documentation across quality assurance processes
Drive continuous optimisation based on process data and trends
Bachelor's degree in Engineering or a related field
Several years of relevant experience as a QA Engineer within the medical device industry, with the ability to operate independently
Strong working knowledge of ISO 13485 and experience in regulated quality environments
Experience with comparable devices, such as Class IIa or IIb medical devices
FDA experience is a plus, though not required
Strong written and verbal communication skills
An open, approachable personality who fits naturally within a relaxed, informal team culture
Comfortable working efficiently under tight timelines with minimal supervision
Be part of a global organisation making a tangible difference in healthcare
Step into a close, collaborative Quality and Regulatory team with real ownership from the start
A permanent role with long-term impact, not a temporary assignment
Reach out to Christian Steenkamp via [staat bij de werkgever] | [staat bij de werkgever]
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Bron
Wij zagen deze vacature op de website van de werkgever. Daar staat de actuele tekst; wijzigingen na 30 juli 2026 zien wij pas bij de volgende controle. Wij hebben deze vacature na het vinden nog niet opnieuw gecontroleerd, dus hij kan inmiddels vervuld zijn.