Quality Assurance Manager

vor 2 Wochen

Zurich, Schweiz Sonova Vollzeit

Who we are

You enjoy creating and innovating. You never stop striving for better. You take responsibility and you get results. You love being part of a team. Above all, you want your work to matter: Welcome to our world At Sonova we create sense by bringing sound to life. Our innovative hearing care solutions help millions of people enjoy life’s unforgettable moments.

We offer exceptional career opportunities through market-leading brands from consumer to medical, products and services that keep pushing hearing care forward, and a culture where you can quickly belong and perform at your best.

If you want the freedom to explore, opportunities to grow, and make positive change on people lives through your work, this is the place for you.

Join Sonova. Create sense.
- Staefa, SwitzerlandQuality Assurance Manager
- We're seeking a dynamic and detail-oriented Quality Assurance Manager to join our team. In this pivotal role, you will be responsible for crafting and enforcing comprehensive quality control systems and procedures to align with regulations, customer expectations, and our own high company standards. This role requires a proactive partner who can effectively lead quality assurance activities, including the initiation of corrective and preventive actions, change management, and addressing non-conformities. Moreover, you will be instrumental in conducting internal audits and offering support during external audits. If you're passionate about ensuring quality at every level of an organization, we'd love to hear from you.**Your tasks**
- Ensure the successful implementation and execution of our Quality Management System
- Manage Corrective and Preventive Actions (CAPAs), document and change control, support product and process non-conformities, and intercompany quality activities
- Conduct internal audits, provide support for external audits
- Inform management about the QMS effectiveness
- Coordinate the creation, monitoring, and control of QM documents and records
- Act as a core team member of internal QM projects and cross-functional working groups
- Collect and evaluate quality data and information
- Contribute to the development of quality goals and processes
- Support and motivate team members to enhance their understanding of the QMS
- Provide quality management training to new employees

**Your profile**
- Degree in engineering, science, or quality, regulatory & compliance disciplines
- At least 5 years of relevant work experience in a GMP environment with a bachelor's degree, or 3+ years of quality experience in a medical device company with a Master’s degree.
- Demonstrated experience in GMP, GDP, ISO 13485, CFR 820
- Ability to manage multiple activities, projects, and priorities
- Self-motivated, flexible, analytical thinker with strong organizational skills
- Excellent communication and presentation skills, both oral and written
- Fluent in English both written and spoken
- Proficient in Quality Management system software, MS Office Suite, and SAP R/3 or S/4

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

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