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Salary
≈ $73k – $169k per year (Estimated)
Location
In office (Germany)
Seniority
Senior · 5+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 1, 2026. First seen by Alion on Jun 5, 2026. Dornier MedTech scores B on the Alion truth index.

Overview
Company
Impact
Profile match
With our commitment to customer-centric innovation, we go beyond to engage with patients and develop excellent end-to-end urology solutions that serve the ever-changing urology landscape. Dornier. Advancing Urology Care with You.

Your mission

Position Summary & Goal

Development, implementation and testing of software for medical products, which represent state-of-the-art technology. Focus is on delivering innovative solutions that meet customer as well as regulatory requirements, particularly those related to safety and effectiveness.

The deliverables contribute to increasing the competitiveness and commercial success of Dornier MedTech and its subsidiaries, particularly DMT Systems. Solutions are provided in a cost- and time-efficient manner and by strong collaboration with stakeholders and cross-functional departments.

Primary Responsibilities:

a) Software development

  • Development, implementation and verification of architecture, concepts and solutions according to product and design specifications
  • Coordination and cooperation with third-party suppliers, contractors and especially GUI designers
  • Supporting project management in planning software-related tasks
  • Collection and determination of technical requirements
  • Support of trouble shooting in production related to software issues
  • Sustaining of existing products / systems to ensure stable and reliable operations a spart of the product lifecycle management process

b) Documentation

  • Adherence of projects goals, national and international standards and regulations (CE, FDA, MDR…),
  • Create documentation according to regulatory requirements in the strongly regulated field for medical devices, like requirements, specifications, risk analysis and verification documents

    Your profile

    • Graduate in engineering or computer science or equivalent
  • Proven working experience of 5 years+ of GUI software engineering in the embedded field
  • Experience in coordinating software-related tasks and assisting with project planning is desirable
  • Experience in a regulated environment, preferably in the field of regulated medical devices or a different domain
  • Experience with Qt/QML
  • Experience with LVGL, TouchGFX, EmbeddedWizard or wxWidgets is a plus
  • Experience with Embedded Linux (Kernel-configuration, driver development, build-systems like Yocto/Buildroot)
  • profound knowledge in Ansi C, C++
  • Profound knowledge with Microcontrollers / Microprozessors
  • Experience with reatlime operating systems - RTOS (FreeRTOS, Zephyr, QNX)
  • Experience with hardware concepts, memory constraints, display controllers, GPU/GPU-less rendering, touchscreen drivers
  • Experience with integrated development environments like Keil, IAR, Code Composer, STM IDE, Cube MX
  • Quick learner
  • proactive attitude and strong teamplayer
  • Systematic work ability and high-quality awareness
  • Regulatory know-how: ISO 13485, FDA 21 CFR 820.30, IEC 62304, IEC 14971
  • Experience with ALM-Tools like DOORS, Polarion or CodeBeamer

• Ms Office (Outlook, Word, Excel, PowerPoint, etc.)

Why us?

  • Personal induction plan and comprehensive onboarding
  • Flexible working hours
  • 30 days of holiday
  • interesting tasks in a dynamic, international environment
  • Continuous training and development
  • Flat hierarchies
  • Attractive canteen
  • Free coffee, tea and water
  • Employee events
  • Charging stations for electric cars
  • Accident insurance
  • Employer contribution to VWL
  • Employee fund with various allowances and subsidies
  • Free language courses
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