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Senior Quality Assurance Officer

Confidential

Utrecht, Utrecht, Netherlands permanent

Posted: March 23, 2026

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Quick Summary

Vitestro is a company that designs and develops an autonomous robotic blood collection device for medical procedures. The job involves working with a team of over 90 people to improve patient experience and address healthcare staffing shortages. A senior quality assurance officer is responsible for ensuring the device is functioning properly and ensuring patient safety.

Job Description

About Vitestro

Founded in 2017 in Utrecht, Vitestro is pioneering the future of blood collection with the Aletta® Autonomous Robotic Phlebotomy Device™ (ARPD™). This groundbreaking medical device combines advanced multi-modal imaging (near-infrared, ultrasound, and Doppler ultrasound) with robotics and AI to perform the entire diagnostic blood draw procedure autonomously.

By addressing critical healthcare staffing shortages and improving patient experience, Vitestro is transforming one of the most common and essential medical procedures. With more than 90 team members and growing rapidly, we are scaling our impact. As we placed our first devices with customers, we are now expanding our team to ensure successful implementation and long-term reliability.

At Vitestro, we are committed to continuous innovation and improvement. Our can-do mentality and passion to work on the toughest challenges to find cutting-edge solutions leads us to a huge success: we are growing fast. And for that, we need your help.

Senior Quality Assurance Officer

As a QA Officer at Vitestro, you will play a crucial role in ensuring compliance with all applicable laws, regulations, and standards within the operations and product development, focusing on Medical Devices manufacturing.

Your timing is perfect: you will be joining Vitestro during a highly interesting period, as the next 12 months will be incredibly important from a quality and regulatory perspective.

Together with our QA/RA team, you will support the maintenance of the QMS by making sure that the whole organization follows the Standard Operating Procedures (SOPs). When you think the SOP can be improved, you will proactively suggest changes to the SOPs. Additionally, you will offer support during QMS audits, both internal as with our notified boy.

For this role you should have the right project management and communication skills to distribute the workload across the organization. You will play a key role regarding quality in the organization. You will perform a wide range of activities, for example: risk management activities, design & development topics, production control, employee training, CAPA management, supplier control, etc.

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