About this role
Our R&D team develops the next generation of Brainlab image-guided surgery and Digital O.R. platforms. These innovative medical devices form the physical foundation for Brainlab current and future software solutions and must meet the highest standards of safety, performance, and regulatory compliance.
As a Senior Project Engineer, you take technical ownership of development projects within our surgical navigation portfolio. Your drive the development from concept through verification to a certified medical product, working in close collaboration with hardware, software, quality, and external partners. The role combines hands-on engineering, technical leadership, and project coordination in a regulated medical device environment.
Depending on experience level, the scope of responsibility may be adjusted. Junior or mid-level engineers with strong technical fundamentals and high development potential may also be considered and will be supported accordingly.
Key responsibilities:
Take technical leadership and contribute to decision-making with targeted creativity and technical expertiseDrive the product requirements engineering process by translating stakeholder input into compliant system, software, and hardware requirements Define, evaluate, and review technical concepts and architectures across disciplines (systems, software, electronics and mechanics)Coordinate internal and external development activities, including suppliers, development partners, and test housesPlan and support prototype build-up, component qualification, and design iterationsDefine, execute, and document verification activities; coordinate interdisciplinary troubleshooting and root‑cause analysis; and drive bug fixes or redesigns toward specification complianceContribute substantially to design and development documentation according to applicable regulations and standardsAct as a technical interface between several contributors, including hardware, software, quality management, and project managementYou will work at the intersection of our platform development team, multiple software teams, regulatory functions, international suppliers and development partners. Clear communication, technical judgment, and structured decision-making are essential to succeed in this role.
University degree in medical engineering, electrical engineering, computer science, software engineering, physics, or a comparable technical fieldSeveral years of experience in medical device or regulated product developmentSolid understanding of system-level thinking and interdisciplinary developmentExperience contributing to development projects within cross-functional teamsStrong technical skills with the ability to discuss details with engineers and align with management on high-level goalsExperience with development documentation and verification activities in regulated environmentsExcellent communication skills in English and GermanWhat sets you apart:
You enjoy taking technical responsibility and driving topics to closureYou are comfortable navigating complex systems and regulatory constraintsYou combine analytical thinking with a pragmatic, solution-oriented mindsetYou communicate clearly across disciplines and organizational boundariesYou are motivated to grow—either as a senior technical contributor or toward broader technical leadershipWe are also glad to interview engaged graduates who want to develop themselves in a successful and international company.
A mutually-supportive, international teamMeaningful work with a lasting impact on medical technology30 vacation days, plus December 24th and December 31stFlexible working hours as well as hybrid work model within GermanyBike leasing via cooperation partner "BikeLeasing"Parking garage and safe underground bike storageAward-winning subsidized company restaurant and in-house cafesVariety-rich fitness program in our ultra-modern 360m2 company gymRegular after work, team, and company eventsComprehensive training and continuing education opportunitiesReady to apply? We look forward to receiving your online application including your first available start date and desired salary.
Contact person: Elisabeth Karro