Verification Engineer (m/f/d)

Verification Engineer (m/f/d)

Position Summary

We are looking for a motivated and skilled Verification Engineer to join our international R&D team in Munich. You will contribute to a high-priority, cross-disciplinary product development project focused on a next-generation Heart-Lung Machine used during cardiac surgery. This life-support system integrates complex software and hardware functionalities, requiring thorough verification at subsystem and system levels.

This role offers the opportunity to grow within a highly regulated and innovative environment, contributing to the development of medical devices that make a real difference in patient care.

General Responsibilities

• Support the development and execution of verification strategies for software-driven electromechanical medical devices at subsystem and system levels.
• Design and execute test cases based on design input requirements and risk analysis.
• Assist in the development and maintenance of test fixtures and test benches for manual and automated testing.
• Participate in the creation and execution of test automation scripts and frameworks.
• Document verification activities in compliance with regulatory standards (FDA, MDR).
• Analyze test results and report defects using structured bug tracking tools.
• Collaborate with cross-functional teams (software, hardware, systems, clinical) to ensure comprehensive verification coverage.
• Contribute to the preparation of verification documentation for regulatory submissions.
• Maintain and improve existing test environments and support their extension as needed.

Skills and Experience

• Master’s degree in (medical) engineering, software engineering, or a related technical field.
• Some years of experience in software and system verification, preferably within the medical device or regulated industry.
• Experience in test design, test execution, and bug reporting.
• Strong analytical skills in understanding requirements and defining accurate test scenarios to ensure high coverage.
• Good documentation skills for preparing V&V documentation aligned with regulatory standards (FDA, MDR).
• Familiarity with automated requirements and test management tools (e.g., Polarion, DOORS).
• Basic experience with test automation tools and scripting (e.g., Python, CAPL, VTestStudio).
• Exposure to CAN-Bus communication and Vector tools (e.g., CANoe, CAPL).
• Understanding relevant standards such as IEC 60601-1 and IEC 62304 is beneficial.
• Experience in test bench or test fixture design, maintenance, and improvement.
• Good communication skills in English (spoken and written); German is a plus.
• Team-oriented, proactive, and eager to learn and grow in a dynamic environment.
• 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!