SEGULA Technologies

https://www.segulatechnologies.com

5001+

Engineering Services

SEGULA Technologies is a global engineering group, serving the competitiveness of all major industrial sectors: automotive, aerospace, energy, rail, naval, life sciences and telecoms. With a presence in over 30 countries and 140 offices worldwide, the Group is committed to building close relationships with its customers through the skills of its 15,000 employees. A leading engineering company with innovation at the heart of its strategy, SEGULA Technologies carries out large-scale projects, from research to industrialisation and production.

More information: https://www.segulatechnologies.com

Job Description

Company Description

Do you want to shape the world of tomorrow and work on innovative projects? Then you're a good fit for us! We are a global engineering group with 15,000 employees and 140 locations worldwide. With our services, we are driving the topics of energy efficiency, climate protection and decarbonization and developing tech industries into new dimensions.

In the United States, the world of SEGULA Technologies Experts revolves around industries such as automotive, software, energy and life sciences. As an independent player, we support OEMs and suppliers with personal engineering services. Take advantage of new opportunities and take on exciting tasks and attractive positions with direct customer assignment.

Job Description

Develop and maintain embedded and application-level software for medical devices in compliance with FDA, ISO 13485, and other regulatory standards.
Design and implement user interfaces using modern UI frameworks (e.g., React, Angular, Qt) while adhering to UI design guidelines.
Perform system-level integration to ensure seamless communication between hardware, firmware, and software components.
Conduct comprehensive software testing and validation, including unit, integration, and system testing, as well as static and dynamic analysis.
Write and maintain Software Design Descriptions (SDDs), test procedures, and validation reports aligned with medical device documentation standards.
Build and package installable software (.spk or similar) and work comfortably with Linux development environments.
Utilize programming skills in Tcl/Tk, C++, Java, and/or Python to support new and legacy codebases.
Handle file system I/O tasks such as USB, CD, and local directory access.
Maintain and support legacy systems, including tool migration and codebase refactoring.
Assist in the interpretation, review, and execution of detailed software and system requirements.
Collaborate cross-functionally with hardware, QA, regulatory, and clinical teams to ensure compliant and high-quality product development.
Participate in Agile or Waterfall lifecycle activities, including sprint planning, backlog grooming, requirement tracing, code reviews, and iterative releases.
Familiarity with tools like AppMan and software development best practices in regulated industries.

Qualifications

7-10 years relevant work experience.
Bachelor's degree in systems engineering or software engineering required.
Strong analytical and problem-solving abilities.
Excellent communication and documentation skills.
Comfortable working cross-functionally with engineering, QA, regulatory, and clinical teams.
Ability to interpret and execute complex requirements with attention to detail.
Knowledge of cloud technologies such as AWS/GCP, or Azure.