Job description
We are seeking a Software Integration Engineer with experience in medical imaging systems, PACS integration, and end-to-end workflow validation. The role focuses on verifying and validating software solutions deployed in clinical environments, ensuring seamless interoperability with PACS, imaging modalities, distributors' ecosystems, and healthcare IT infrastructures.
The successful candidate will be responsible for planning and executing integration and validation activities, assessing system behavior across complete processing chains, and ensuring that clinical workflows operate reliably in real-world environments.
Responsibilities
Verify interoperability between the software solution and external healthcare systems
Validate end-to-end imaging workflows from image acquisition through processing, storage, review, and reporting.
Perform integration, system, workflow, regression, and user acceptance testing in representative customer environments.
Assess product performance and behavior across different deployment configurations and clinical use cases.
Plan, design, and execute integration and validation activities for medical imaging software in compliance with IEC 62304 and applicable regulatory requirements.
Contribute to risk-based verification and validation activities in accordance with ISO 14971.
Ensure traceability between requirements, risks, test evidence, and validation reports.
Collaborate with development, regulatory, clinical, product management, and distributor teams to address issues and improve product quality.
Participate in continuous improvement of validation methodologies, test environments, and test assets.
Key Tasks
Develop and implement integration and validation plans & reports
Execute manual and automated validation activities covering operational workflows with different third-party applications and platforms.
Validate DICOM interoperability, image exchange, storage, routing, and retrieval workflows.
Verify software installation, configuration, upgrade, and deployment procedures.
Reproduce and investigate customer-reported issues in integrated environments.
Analyze defects, perform root-cause investigations, and support corrective and preventive actions.
Conduct risk-based testing based on intended use, clinical impact, and workflow criticality.
Generate objective evidence required for audits, regulatory submissions, and product releases.
Support validation activities with distributors, partners, and customer sites.
Maintain test environments representative of real-world healthcare deployments.
Job requirements
Education
Bachelor's or Master's degree in:
Biomedical Engineering
Computer Science
Medical Imaging
Software Engineering
Healthcare Information Systems
Related technical discipline
Experience
3 to 7 years of experience in software development, validation, verification ( or quality assurance).
Experience with medical devices and regulated environments strongly preferred.
Experience with PACS, DICOM, RIS, VNA, or enterprise imaging solutions.
Experience validating integrated healthcare solutions in customer or production-like environments.
Exposure to AI-based medical imaging applications is an asset.
Knowledge
Medical Device Software Lifecycle (IEC 62304)
Quality Management Systems (ISO 13485)
Risk Management (ISO 14971)
MDR and/or FDA regulations
DICOM, PACS, RIS, HL7, and healthcare interoperability concepts
Client-server architectures and healthcare IT infrastructures
Validation and verification methodologies
Jira, Xray, Confluence, Git
Preferred:
Knowledge of cloud-based healthcare platforms
Kubernetes, Docker, Azure environments
Basic understanding of automation and scripting for validation activities
Skills
Software development & scripting
System Validation
Integration Testing
PACS & DICOM Workflow Validation
Defect Investigation and Root Cause Analysis
Excellent communication with technical and non-technical stakeholders
Fluent english
Personal Qualities
Rigorous and quality-focused
Analytical and methodical
Autonomous and proactive
Detail-oriented while maintaining a system-level perspective
Strong collaboration and communication skills
Comfortable interacting with customers, distributors, and cross-functional teams
Able to work effectively in a regulated healthcare environment
Median Technologies is committed to cultural diversity, gender equality and the employment of disabled workers.
- Valbonne, Provence-Alpes-Côte-d’Azur, France
or
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