(Summary generated by AI based on the full job description)
The project involves developing software for medical devices in a strictly regulated environment. Key technologies include Azure DevOps, YAML, VectorCAST, SonarQube, Black Duck and tools for regulation-compliant CI/CD. Responsibilities cover designing and maintaining automated CI/CD pipelines, integrating testing tools, and ensuring compliance with FDA and MDR standards. Knowledge of IEC 62304 and ISO 13485 standards and managing change processes with audit documentation is required.




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