Experteer Overview
In this role you ensure the safety, performance, and compliance of PDM software by designing verification tests and maintaining rigorous traceability. You collaborate with developers, systems engineers, and product teams to secure comprehensive verification coverage in a regulated medical-device context. You will shape test strategies for complex features and report results to enable high-quality software releases. This position offers a chance to contribute to patient outcomes in a global, innovation-driven company.
Retribuzione / Benefits
- Analyze requirements for testability and provide improvement feedback
- Define and document test scenarios and cases aligned with system functionalities
- Design and execute verification tests and document results
- Maintain traceability between requirements, test cases, and results
- Identify, document, and track software anomalies and perform root cause analysis
- Contribute to test strategy for complex features including environments, tools, and interfaced systems
- Collaborate with developers, system engineers, and product teams to ensure verification coverage
- Report testing activities, results and anomalies using Azure DevOps
Responsabilità
- 3+ years of software testing for desktop applications and distributed systems
- Strong knowledge of requirements engineering with ability to review and trace specifications
- Proven track record of creating/maintaining test plans, test cases, and traceability matrices for functional, non-functional, UI, integration, and regression testing
- Experience with Azure DevOps, JIRA, or similar for planning, execution, defect tracking, and CI
- Skilled in analyzing logs, network traces (Wireshark/Fiddler), and system event logs for root cause analysis
- Working knowledge of SQL Server and writing/executing complex T-SQL for data validation and backend testing
- Experience in test data anonymization, HIPAA/GDPR considerations, and PHI handling
- Hands‑on medical device software verification experience with IEC 62304, ISO 14971, ISO 13485, FDA 21 CFR Part 11
- Experience in Agile and hybrid environments, sprint testing, risk-based testing, and DevOps pipelines
- Bonus: familiarity with HL7, FHIR, DICOM
- Fluent English
- Multicultural collaboration mindset with results orientation
