Job Description You will contribute to the development and enhancement of our company-wide software platform, playing a key role in implementing a state-of-the-art technology platform for software development in our medical GMP (Good Manufactory Process) and RUO (Research Use Only) instruments. In this role, you will take on significant technical responsibilities and act as a key point of contact for collaboration with various teams and stakeholders. You actively contribute to the development and implementation of the platform roadmap by collaborating closely with project and program managers, software architects, product owners, requirements engineers, UX/UI designers, software developers, and testers, while also taking responsibility for the platform's technical advancement to ensure that defined goals are achieved on time and with high quality. You leverage your expertise to continuously improve the software platform and develop new and innovative solutions that are utilized across various software products. You write clean, maintainable and scalable code in C++ and share your knowledge with the team. You collaborate closely with other departments in our interdisciplinary and international environment, including other software development teams, biologists, IT, Quality, Service, and Marketing. You support communication with external stakeholders, contribute to critical business decisions, and provide input and ideas to shape the future of our global software development organization.