Sr System Quality 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.

Tests product and/or solution functionality; analyzes and debugs e.g. software related product issues.

The Senior System Quality Engineer (SQE) ensures that software within a regulated medical device environment is verified to meet functional, safety, quality, and regulatory requirements across the entire product lifecycle.

In this role, you will drive and contribute to planning, designing, executing, and documenting verification activities, working closely with development, systems engineering, product management, and quality/regulatory stakeholders.

You will also play a key role in optimizing verification strategies, ensuring an efficient and sustainable product development.

Your Key Responsibilities

Verification Excellence

• Plan, design, execute, and document manual and automated verification tests for medical device software
• Ensure coverage of system requirements and risk controls in line with internal PLC processes
• Deliver complete, traceable, and audit‑ready verification documentation aligned with the QMS
• Support defect investigation, risk assessment, and verification of corrective actions

Test Strategy & Traceability

• Contribute to verification strategies, test plans, and impact analyses
• Maintain full traceability across requirements, risks, test cases, and results
• Participate in readiness reviews (test readiness, release readiness, etc.)

Cross-Functional Collaboration

• Collaborate closely with developers, system engineers, testers, and clinical/UX experts
• Clearly communicate test progress, risks, and quality assessments to stakeholders

Your Impact Beyond Execution

• Drive optimization of verification efforts across the product landscape
• Apply risk-based testing strategies, focusing on high-impact areas
• Continuously improve verification approaches, balancing manual and automated testing
• Act as a cross-team coordinator, aligning verification practices across teams
• Promote efficiency, consistency, and sustainability in testing processes

Your Profile

• Strong experience in software verification within a regulated environment (medical devices preferred)
• Experience with test strategy, traceability, and risk-based testing approaches
• Strong analytical mindset and structured way of working
• Excellent communication and stakeholder management skills
• Ability to work effectively in cross-functional, international teams

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 applicat