Test and Verification Engineer (Medical Device Software)

About the role

As a Test and Verification Engineer you will ensure the reliable operation and regulatory compliance of Artidis' medical‑device software. You will plan and execute verification testing, support requirements engineering and analyse anomalies, working closely with software, mechatronics, validation and backend teams.

Key responsibilities

• Create and review test and validation protocols based on requirements, change records and anomaly reports.
• Conduct verification, regression and system testing and maintain auditable test results.
• Design, implement and validate script‑based automated testing processes.
• Maintain change records, traceability matrices and collaborate with regulatory teams to meet FDA and other standards.
• Generate technical reports, release documentation and compliance records.

Required profile

• Bachelor’s degree in software engineering or equivalent.
• At least 3 years of experience in medical‑device or other highly regulated software development.
• Experience with complex hardware such as robotic or embedded systems is a strong plus.
• Proven ability to work independently in a fast‑paced, agile environment.
• Excellent written and spoken English.

Required skills

• C/C++ programming.
• Python scripting and use of Large Language Models for code creation and documentation.
• AWS cloud services.
• CI/CD pipeline implementation.
• IoT device management and DevOps practices.
• Software troubleshooting, analysis and debugging.

What we offer

• Competitive salary with performance‑based bonus.
• Rapid career advancement in a high‑impact health‑tech startup.
• Agile, international team with opportunities to shape testing methods and automation frameworks.
• Hybrid work model – primarily onsite with limited remote flexibility.