QA Engineer

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

At our R&D site in Dättwil, Switzerland, with more than 400 employees, mostly engineers, computer scientists and physicists we specialize in the development of imaging software and hardware as well as treatment management systems for radiation therapy cancer treatment. Bring your talent to a place where your work will help fight cancer.

As a Supplier Quality Engineer, you are accountable that our suppliers deliver quality parts, materials, and services according to company standards. You keep abreast of regulatory procedures and changes and interact with our suppliers and manufacturing to ensure compliance throughout the complete supply chain.

You work in close collaboration with other teams and stakeholders in Europe and overseas.

Finally, due to the safety critical nature of radiation therapy, your commitment to quality is a must.

Main Responsibility

• Ensures compliance requirements according to Medical Device Regulations ISO 13485, and the company quality manual
• Ensures that suppliers deliver quality parts, materials, and services
• Reviews and approves final product quality acceptance
• Administrates and monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur
• Generates analysis of the returns of non-conforming parts
• Support the supplier evaluation to assess their overall performance and provides feedback in assessment of their operation
• Supports and evaluate manufacturing issues with root cause analysis and corrective actions implementation
• Ensures in close collaboration with manufacturing that all production processes are compliant
• Qualifies suppliers according to company standards
• Perform supplier audits

Requirements

• Completed technical education with further training in the quality area
• Experience in quality assurance and working with regulations
• Used to working independently and communicative
• Fluence in German, written and verbal, is mandatory, English is preferred
• Experience in supplier auditing preferred
• Min. 3 days per week onsite

Who we are : We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.

How we work : When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

To find out more about Healthineers’ specific businesses, please visit our company page here.

As an equal opportunity employer, we welcome applications from individuals with disabilities.

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