.Based in Malaga, D.Med Software S.L.U. is an integral part of the globally renowned D.Med Healthcare Group, headquartered in Düsseldorf, Germany. We began as a small team of passionate developers and have rapidly grown into a dynamic company specializing in advanced software systems for the medical industry. D.Med Software specializes in providing cutting-edge cybersecurity solutions tailored specifically for the embedded systems in the medical industry. As a leading software service provider, we are committed to revolutionizing healthcare by safeguarding medical devices and enhancing patient care through innovative software technologies. With a wealth of experience in working with ISO 13485 Quality Management Systems, coupled with a proven track record of manufacturing numerous FDA-registered and CE-marked medical devices, we guarantee the compliance of our customers' products with international standards. Our primary mission is to empower our clients to succeed by providing them with unparalleled cybersecurity solutions and fostering long-term partnerships built on trust and reliability. Join our team of dedicated professionals with over 80 years of combined experience in software engineering, medical expertise, and sales. Together, we strive to bring innovative projects to life and achieve market success for our clients. Be part of a company that is shaping the future of medical software! We are looking for a Senior Test Engineer to join our team and lead quality testing in embedded medical devices, ensuring that our products meet the highest standards of safety and performance. This is an exciting opportunity for you career professional to contribute to the growth of our company and gain valuable experience in the healthcare engineering sector. Senior Test Engineer (m/f/d) Your tasks Contribute to the whole life cycle of the software development process with a strong focus on testing and validation. Design, plan, and execute hardware and software tests for embedded medical devices, ensuring compliance with industry-specific regulations and standards. Develop and document test cases, test plans, and validation protocols to ensure system functionality and quality. Coordinate and perform product verification and validation testing at different development phases (unit, integration, and system testing). Collaborate with development, engineering, and product teams to identify issues, conduct root cause analysis, and propose improvements and corrections. Requirements Over 5 years of experience in embedded systems and platform integration testing. Familiarity with test automation tools and frameworks. Proven expertise in system and software validation. Competence in C/C++ and Python. Familiarity with regulatory requirements and industry standards for medical device software (e.G., IEC 62304, FDA guidelines) is highly desirable. Well-founded knowledge in agile software approaches, preferably SCRUM, is desired