Test and Verification Engineer

About Artidis Artidis is a pioneering clinical stage health technology company that aims to set the gold standard in tissue analysis and therapy optimization. By combining its nanotechnology platform for rapid tissue analysis with a holistic data solution, Artidis accelerates drug discovery, tissue engineering, and personalized treatment. Artidis focuses its research and development efforts on solid tumors to enhance responses to chemo, immuno, and cell therapies, driving precision in cancer care. Job Purpose As a Test and Verification Engineer, you'll play a crucial role in ensuring the reliable operation and regulatory compliance of our devices. You will ensure that the software of our medical device works correctly and performs according to the expectation of the medical professionals who will use the device. Your responsibilities will range from planning and executing software verification testing, to supporting software requirements engineering and resolving anomalies through in-depth analysis. You will collaborate daily with our software, mechatronics, validation, and backend teams. Additionally, you will support our production, validation, and service teams in establishing and maintaining test and qualification procedures, be it for manual testing or script-driven, automated testing. Your in-depth engineering know-how will also allow you to understand, challenge and revise our testing methods and our test automation framework. Duties and Responsibilities Create and review software test and validation protocols based on software requirements, change records, and software anomaly reports. Conduct software verification testing, regression testing and system testing, and establish auditable records of the results. Establish test strategies and new software testing processes. Design, implement and validate script-based automated testing processes. Drive the continued integration of AI based review and test processes into our software development and documentation workflows. Maintain change records and software traceability matrices (mapping verification test results to software requirements). Collaborate with regulatory teams to ensure that software changes adhere to industry regulations and standards, including FDA guidelines. Generate technical reports, software release documentation, and compliance records. Work within the Medical Device Software Team to support the execution of development projects from concept phase to completion of verification. Provide insights and feedback to the Medical Device Development Team on software performance and user experience. Qualifications Bachelor’s degree in software engineering or equivalent technical certification. +3 years of experience in medical device development or other strongly regulated industry. Experience in working with complex hardware (e.g. robotic systems, computer vision products or embedded devices) is a strong plus. Experience in C/C++, AWS, CI/CD…