Job Description
Company Description
Founded in 2020 and headquartered in Munich, Snke is transforming healthtech with scalable, data-driven innovation powered by AI and big data analytics. We’re experts specializing in large platforms, digital health and software-driven medical technology. By delivering a trusted orchestration layer, Snke empowers healthcare providers, societies, registries, agencies and all partners to deploy cutting-edge solutions for safe and efficient interventions and enhances patient outcomes. Beyond our Munich headquarters, we have core teams in Chicago, Heidelberg, San Diego and Tel Aviv. Snke fosters global collaboration to create technologies that are smart, enabling and holistic-helping healthcare providers deliver meaningful change.
Snke Theater is a scalable platform to digitize the operating room across clinical applications. We develop a platform to capture structured clinical data, manage and route data and applications, and support the surgical team by bringing together the many sources of information in the operating room into a single environment and replacing the fragmented stack of standalone systems found in most operating rooms today.
Job Description
As a Project Engineer in the Snke Theater division, you will be involved in the development of complex medical software solutions, from early ideas until the final product launch. You will bridge the gab between project management, product owner, developers and other stakeholders. Your focus will not be writing production code, but ensuring that the software solutions and systems meet our high technical, regulatory and quality standards. You will also have the opportunity to collaborate with healthcare professionals to better understand their needs and to develop new solutions that address their most pressing challenges.
- Coordination of medical software development within a cross-functional team, including project managers, developers, and key stakeholders (QM, Usability, QA, and external partners)
- Full responsibility within a defined project
- Support compliance with processes as well as regulatory, data protection and security standards
- Support regulatory activities like CE clearance and FDA submissions
- Creation and maintenance of comprehensive technical documentation in accordance with international and company standards
- Define and coordinate testing activities in cooperation with R&D and QA, including interpretation and documentation of results
Qualifications
- Degree in engineering, natural sciences, medicine, or a related field
- Solid general IT knowledge with a strong affinity for software and software development
- Professional experience at an advanced level, typically including at least 2 years in a relevant role
- Experience in R&D environments, ideally within a regulated industry
- Sound understanding of cloud-based software systems and architectures
- Strong organizational skills with a structured and methodical working style
- High quality standards and a strong focus on structured documentation, regulatory compliance, and accurate project tracking
- Excellent communication and collaboration skills in cross-functional environments
- Fluency in English; German language skills are an advantage
Additional Information
- A supportive, international team connected by shared values and a culture of trust
- Meaningful responsibilities with a lasting impact on global healthtech, improving medical decisions and patient outcomes
- 30 vacation days, plus December 24th and December 31st
- Flexible working hours and a hybrid work model within Germany
- Bike leasing via our partner “BikeLeasing”
- Parking garage and secure underground bike storage
- Subsidized company restaurant and in‑house café
- Urban Sports Club membership with employer contribution
- Regular after‑work, team, and company events
- Centrally located, modern workspace with a 212 m² rooftop terrace
Ready to apply? We look forward to receiving your online application including your first available start date.
Contact person: Tatjana von Freyberg
