Senior DevOps Engineer: Medical Devices & Embedded Systems

GlobalLogic Inc.; United States; On-site; USD 140,000 - 150,000; Full time

Benefits offered by this job

Exciting Projects

Collaborative Environment

Work-Life Balance

Professional Development

Excellent Benefits

Job summary

GlobalLogic, a leading global medical device software partner, is seeking a Principle DevOps Engineer to design, automate, and maintain CI/CD pipelines for embedded medical device software in a regulated environment. You will work with engineering and regulatory teams to ensure end-to-end traceability, tool validation, and compliant delivery in a fast-paced healthcare setting.

Based in Waltham, MA, the role offers challenging projects, competitive compensation, and opportunities for professional

Qualifications

• Minimum of 10 years of DevOps experience in regulated environments.
• Strong security, threat modeling and DevSecOps tooling knowledge.
• Experience configuring and managing CI/CD toolchains (Jenkins, GitLab CI, GitHub Actions, Azure DevOps).
• Embedded build automation experience for embedded/hardware systems (CMake, Make, Docker).
• Experience with static analysis tools integration (SonarQube, Coverity, Klocwork, Cppcheck).
• Familiarity with ISO 13485, IEC 62304, FDA 21 CFR Part 11 and tool validation processes.
• Proficiency in Python, Bash or PowerShell for automation.

Responsibilities

• Architect, optimize, and manage CI/CD pipelines and developer toolchains.
• Configure and automate firmware/software builds for embedded hardware.
• Integrate static analysis and automated testing within the CI toolchain.
• Ensure tool validation and regulatory compliance for all build environments.
• Generate validation reports and documentation for regulatory audits.

Skills

CI/CD Tools

DevOps

Healthcare-Medical Devices

Tools

SonarQube

Black Duck SCA

Artifactory

GitHub Enterprise

Jenkins

Job description

GlobalLogic, a leading global medical device software partner, is seeking a Principle DevOps Engineer to design, automate, and maintain CI/CD pipelines for embedded medical device software in a regulated environment. You will work with engineering and regulatory teams to ensure end-to-end traceability, tool validation, and compliant delivery in a fast-paced healthcare setting.

Based in Waltham, MA, the role offers challenging projects, competitive compensation, and opportunities for professional