Quality Engineer / Quality Engineeress

Quality Engineer

80%-100%, Zurich, fixed-term

At Versive, we are transforming manual wheelchair use with our patented steering-by-leaning system, making propulsion up to twice as efficient, enabling easy one-handed propulsion, and delivering a smooth, intuitive movement experience.

We started as a Wyss Zurich Project in 2025 and are now expanding our team to bring this groundbreaking technology to market. If you are passionate about impactful design, inclusive technology, and meaningful innovation, we would love to hear from you!

Project Background

The Wyss Zurich Translational Center (Wyss Zurich) is a unique accelerator, embedded within ETH Zurich and the University of Zurich, dedicated to emerging fields such as regenerative medicine, robotics, and medical devices/bionics technologies. It was established by a generous donation from Swiss entrepreneur and philanthropist Dr. Hansjörg Wyss to foster translational projects from ETH Zurich and/or the University of Zurich. Wyss Zurich supports projects focusing on developing treatment protocols and clinical therapies, as well as novel technologies and intelligent systems.

Job Description

As our Quality Engineer, you will work closely with the R&D team to lead our testing and quality assurance efforts. You will drive the implementation of our Quality Management System (QMS) and ensure our Class I medical devices meet the highest standards of quality, safety, and regulatory compliance.

You will also help shape our agile startup culture and champion a shared commitment to delivering impactful, user-centered solutions.

Responsibilities:

• Implement and maintain a QMS compliant with ISO 13485, in collaboration with Wyss Zurich QM experts
• Drive requirements engineering in close alignment with R&D
• Lead risk management activities, including risk assessments and mitigation planning
• Oversee and perform in-house durability testing of our wheelchairs
• Plan and coordinate usability and clinical evaluations
• Prepare and maintain technical documentation for CE marking
• Liaise with external regulatory partners to ensure alignment during development

Profile

• Bachelor's or Master's degree in engineering, life sciences, health sciences, or a related field
• 3-5 years of hands-on experience in medical device development
• Solid knowledge of ISO 13485 and related regulatory frameworks
• Experience with CE marking or FDA clearance for Class I medical devices (preferred)
• Training or experience in design, manufacturing, or quality control is a plus
• Strong communication, problem-solving, and team collaboration skills
• Experience in regulatory affairs is an advantage
• Fluent in English; additional languages are a plus
• Self-motivated, adaptable, and excited about working in a startup environment
• Willing to work on-site in Zurich

Workplace

Join a motivated, mission-driven team dedicated to improving lives, in a culture of continuous learning, experimentation, and innovation.

We Offer

• The chance to shape a growing company from the ground up
• An inclusive, supportive work environment with strong team spirit
• Benefits aligned with the ETH Zurich employee benefits program

We Value Diversity

In line with our values, ETH Zurich encourages an inclusive culture. We promote equality of opportunity, value diversity, and nurture a working and learning environment in which the rights and dignity of all our staff and students are respected. Visit our Equal Opportunities and Diversity website to find out how we ensure a fair and open environment that allows everyone to grow and flourish.

Curious? So Are We.

We look forward to receiving your online application. Apply online using the form below. Our review process will prioritize candidates whose applications match the job profile.

About ETH Zürich

ETH Zurich is one of the world’s leading universities specializing in science and technology. Renowned for our excellent education, cutting-edge fundamental research, and direct transfer of new knowledge into society, we foster independent thinking and an inspiring environment that encourages excellence. Located in the heart of Europe yet forging connections worldwide, we work together to develop solutions for the global challenges of today and tomorrow.