Senior Verification Engineer (m / f / d) - Qualitätsmanagement, IT

General Responsibilities

• Develop and implement robust verification strategies for software-driven electromechanical medical devices at subsystem and system levels.
• Lead the creation, review, and optimization of reusable test cases and verification protocols, ensuring alignment with regulatory standards (FDA, MDR).
• Design and develop test fixtures and test benches based on design input requirements to support automated and manual testing.
• Drive the development and integration of test automation frameworks and tools to improve efficiency and coverage.
• Create and manage detailed verification schedules, ensuring timely execution and reporting of results.
• Perform statistical analysis, sample size justification, and test method validation to support verification activities.
• Collaborate closely with cross-functional teams (systems, software, hardware, clinical) to ensure comprehensive risk and safety mitigation.
• Provide technical leadership and mentorship to junior engineers, fostering a culture of excellence and continuous improvement.
• Coordinate verification activities across multiple teams and projects, ensuring consistency and compliance with internal and external standards.
• Contribute to the development and maintenance of documentation for regulatory submissions.
• Support the evolution of the V&V framework and best practices across the organization.

Skills and Experience

• Master’s degree in (medical) engineering, software engineering, or a related technical field.
• Several years of experience in software and system verification, preferably within the medical device industry.
• Proven experience in test design, test execution, and anomaly reporting.
• Test bench or test fixture design, maintenance, improvement, and extension.
• Strong analytical, conceptual, and problem-solving skills.
• High documentation standards for preparing required V&V documentation aligned with regulatory standards (FDA, MDR).
• Hands‑on experience with automated requirements and test management tools (e.g., Polarion, DOORS).
• Proficiency in test automation tools and scripting (e.g., Python, CAPL, VTestStudio).
• Experience with CAN‑Bus communication and Vector tools.
• Familiarity with regulatory standards such as IEC 60601‑1, IEC 62304, and 510(k) submissions is a plus.
• Excellent communication skills in English (spoken and written); German is a strong plus.
• Self‑motivated, proactive, and capable of working independently and in teams.
• Travel 5%

What we can offer you

In addition to providing you with a supportive, inclusive and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with the following :

• A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth
• Exposure to a State‑of‑the‑Art medical device development process, in close co‑operation with international clinicians
• Competitive base salary
• Variable short‑term & long‑term incentives
• Recognition : through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements

If you like the sound of the above and feel energized by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!