Who we are

In a life without sound, our work provides meaning. As a leading provider of innovative hearing care solutions, we are not just a company that makes products: we are a team on a mission to help people enjoy the delight of hearing. To enable a life without limitations, we – through our core business brands Phonak, Unitron, Hansaton, Advanced Bionics and AudioNova – develop, manufacture and distribute solutions that push the limits of technology and redefine the future of our industry.

Staefa, Switzerland

Quality & Process Specialist (temporary 6 months)

The Quality & Process Specialist support the team Corp. ME in regards of quality aspects (QMS) and MDR, MDSAP / ISO 13485 / ISO 9001 requirements, translating them into our engineering environmental, considering our needs and supporting our Corp. ME vision. The ME team is the connection between our R&D and our production. The team develop the production processes, define the production set-up including all equipment, tools and documentation. After implementation in our global production network ME support all production sites in all technical and quality related questions.

Your tasks

• Guidance and improvement of processes, including corresponding descriptions, considering constant monitoring of changes within regulatory aspects


• Training / support of new employees within Corp. ME in the area of high level Corp. ME Quality & Process landscape


• Quality assurance for project deliverables related to our process landscape


• Support project leaders, engineers and developers with interpretation and implementation of different standards, guideline and regulatory aspects


• Active contribution during audit preparation and also while audit gets executed, can also include explanations in front of the auditor


• Support and execute related NCs and CAPAs

Your profile

• Degree in Engineering and / or Quality & Regulatory Management


• Experience working in the area of process development, product industrialization or product development preferably in a medical devices environment


• Knowledge in regulatory and quality management is a must (MDR, FDA 21 CFR 820, ISO13485)


• Committed and quality oriented person combined with good communication skills


• Fluent German and good English skills (written and spoken)


• Very command of MS Office programs

Our offer

We can offer you a new challenge, with interesting tasks and much more – including an open corporate culture, flat hierarchies, support for further training and development, opportunities to take on responsibility, an excellent range of foods, sports and cultural facilities, attractive employment conditions, and flexible working time models in various roles.

Daryl Alther, Talent Acquisition Manager, is looking forward to receiving your complete application (CV, references and certificates) via our online job application platform.

For this vacancy only direct applications will be considered. 

Sonova AG
Laubisrütistrasse 28
CH-8712 Stäfa
+41 58 928 01 01

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.