Senior DevOps Engineer, Embedded Medical Devices (Remote)

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

Job summary

GlobalLogic is seeking a skilled DevOps Engineer to join our development team supporting our client. You will design, maintain, and automate modern CI/CD infrastructure tailored for embedded systems and medical device software, ensuring regulatory compliance.

You will collaborate with engineering and regulatory teams to ensure pipeline stages are robust, automated, and fully validated in accordance with medical device standards. This role offers competitive pay and benefits.

Qualifications

• 10+ years of DevOps experience in regulated settings.
• Cloud environments for regulated medical devices.
• Strong security practices and DevSecOps tools.
• CI/CD toolchains: Jenkins, GitLab CI, GitHub Actions, or Azure DevOps.
• Embedded build environments with CMake, Make, Docker, GCC/Clang.
• Quality tools integration: SonarQube, Coverity, Klocwork, or Cppcheck.
• Regulatory awareness: ISO 13485, IEC 62304, FDA 21 CFR Part 11.
• Scripting: Python, Bash, PowerShell.

Responsibilities

• Architect, optimize, and manage CI/CD pipelines and toolchains.
• Configure and automate firmware/software builds for embedded devices.
• Integrate static analysis tools and automated testing in CI.
• Ensure tool validation and regulatory compliance.
• Document validation plans and generate regulatory reports.

Skills

CI/CD Tools

DevOps

Cloud Environments

Regulated Medical Devices

Security Practices

DevSecOps Tools

Python

Bash

PowerShell

Automation

Tools

Jenkins

GitLab CI

GitHub Actions

Azure DevOps

SonarQube

Black Duck SCA

Artifactory

GitHub Enterprise

Docker

CMake

Make

GCC/Clang

Job description

GlobalLogic is seeking a skilled DevOps Engineer to join our development team supporting our client. You will design, maintain, and automate modern CI/CD infrastructure tailored for embedded systems and medical device software, ensuring regulatory compliance.

You will collaborate with engineering and regulatory teams to ensure pipeline stages are robust, automated, and fully validated in accordance with medical device standards. This role offers competitive pay and benefits.