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Tier-1 employer, mid-level DevOps title, metro location, and 5+ years experience create high competition.
Strong medical-device regulatory, MISRA/SAST, and HIL/SIL requirements make background fit highly industry-specific.
Multiple mandatory tech stacks plus IEC 62304/FDA compliance and explicit 5+ years requirement increase candidate filtering strictness.
Design, automate, and maintain end-to-end CI/CD pipelines in a regulated medical device software environment adhering to IEC 62304 and FDA standards.
Automate compliance reporting, code quality gates (MISRA/SAST), and audit trail documentation to assure strict regulatory compliance.
Integrate software-in-the-loop (SIL) and hardware-in-the-loop (HIL) testing environments into CI/CD workflows and manage multi-platform build orchestration, artifact lifecycle, and observability dashboards.
Bachelor's degree in Computer Engineering or Computer Science.
5+ years of experience in building CI/CD pipelines with DevSecOps and compliance-as-code practices.
Proficient with Infrastructure as Code tools (Terraform, Ansible, CloudFormation) and platforms including Docker, Git/GitHub, JFrog Artifactory, AWS, Azure DevOps, Kubernetes.
Strong experience in regulated industries or equivalent - specifically medical device software compliance with IEC 62304 and FDA requirements.
Experienced individual contributor capable of independently designing and managing complex, compliant CI/CD and automation pipelines in a medical device or similarly regulated environment.
Demonstrates deep technical expertise in multi-platform embedded firmware build environments and bridging digital and physical testing (SIL/HIL).
Skilled in automating DevOps workflows to ensure traceability, audit readiness, and operational excellence with minimal supervision.