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At Sonova, we envision a world where everyone can enjoy the delight of hearing. This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection - from personal audio devices and wireless communication systems to hearing aids and cochlear implants. We're dedicated to providing outstanding customer experiences through our global audiological care services, ensuring that everyone has the opportunity to engage fully with the world around them.
Guided by a culture of continuous improvement that fosters resilience and self-motivation, our team is united by a shared commitment to excellence and a deep sense of pride in our work, each of us playing a vital role in creating meaningful change,
Here you’ll find a diverse range of opportunities that span both consumer and medical solutions and the freedom to shape your career while making an impact on the lives of others. Join us in our mission to create a more connected world, where every voice is heard and every story matters.
Design Quality Assurance Engineer (Senior) 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 (Senior), 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
Ensure compliance of R&D processes with internal and external regulations
Support definition of user needs and design validation activities
Support with design FMEA activities and to identify critical to quality attributes
Support design control activities for new development projects (Hardware/Software)
Collaborate with development teams to prevent/identify quality issues early
Support design changes and post-launch improvements
Contribute to process harmonization and standardization across R&D
Assist with audits, NCs, CAPAs, and quality documentation as required
Your Profile
5+ years of 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, ISO 14971, and MDR 2017/745
Hands-on experience with software development, IEC 62304/1, IEC60601 series is a plus
Hands-on experience with design control, product risk management and design FMEA
Excellent communication and stakeholder management skills
Proficient in MS Office; experience with tools like Visio, Project, or Polarion is a plus
Detail-oriented, organised, and confident in influencing without authority
Fluent in English; German is a plus
Sonova is an equal opportunity employer. We team up. We grow talent. We collaborate with people of diverse backgrounds to win with the best team in the market place. We guarantee every person equal treatment in regard to employment and opportunity for employment, regardless of a candidate’s ethnic or national origin, religion, sexual orientation or marital status, gender, genetic identity, age, disability or any other legally protected status.
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