Join Sonova’s global quality team and play a key role in ensuring our innovative medical devices meet the highest standards of safety, performance, and compliance. As a Design Quality Assurance Engineer, you’ll partner with R&D teams to guide product development from concept to launch, ensuring regulatory excellence every step of the way.
Key Responsibilities
* Support design control activities for new development projects (Hardware/Software)
* Perform risk management activities for assigned projects
* Support with design FMEA activities
* Actively collaborate with cross-functional development teams
* Support design changes and post-launch improvements
* Contribute in continuous improvement projects
Your Profile
* Proven practical experience in a regulated industry, preferably medical devices
* Bachelor’s or master’s degree in engineering, science, quality is a plus
* Knowledge of ISO 13485 and ISO 14971
* Hands-on experience with design control, product risk management and design FMEA
* Hands-on experience with software development, IEC 62304/1, IEC60601 series is a plus
* Proficient in MS Office; experience with tools like Visio, Project, or Polarion is a plus
* Fluent in English
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