Principle DevOps Engineer (Medical Devices & Embedded Systems)

Hi Associate,

Greetings for the day,

We have a position as a Principle DevOps Engineer (Medical Devices & Embedded Systems) role in Waltham, MA. Please find the job description below for this position.

Role: Principle DevOps Engineer (Medical Devices & Embedded Systems)

Location: Waltham, MA

Duration: 24 Months

Job Description:

• Strong foundational knowledge of general security practices, threat modeling, and DevSecOps tools (e.g., SonarQube, Black Duck SCA, Artifactory, GitHub Enterprise, and Jenkins) embedded within deployment workflows.
• DevOps Expertise: Strong experience setting up and managing CI/CD tools (e.g., Jenkins, GitLab CI, GitHub Actions, or Azure DevOps).
• Embedded Software Build Environments: Hands-on experience with build automation tools (e.g., CMake, Make, Docker, GCC/Clang toolchains) for embedded or hardware-centric systems.
• Quality Tools Integration: Experience integrating static analysis tools (e.g., SonarQube, Coverity, Klocwork, or Cppcheck).
• Regulatory Awareness: Familiarity with regulated industry standards (e.g., ISO 13485, IEC 62304, FDA 21 CFR Part 11) and formal tool validation processes.
• Scripting Skills: Proficiency in scripting languages such as Python, Bash, or PowerShell for build and task automation.

Job Responsibilities:

• CI/CD Pipeline Management: Architect, optimize, and manage continuous integration and deployment (CI/CD) pipelines and developer toolchains.
• Embedded Build Systems: Configure and automate firmware/software builds specifically for target hardware and embedded device environments.
• Quality & Static Analysis: Integrate and maintain static code analysis tools, liners, and automated testing suites within the CI toolchain.
• Validation & Compliance: Ensure all build tools, environments, and pipeline components meet software tool validation requirements under medical device regulatory frameworks.
• Documentation & Reporting: Execute approved validation plans and generate technical validation reports required for regulatory audits.

Department/Project Description:

Project Overview:

The customer is a global medical device company developing point-of-care diagnostic systems used in hospital and clinical environments. The project focuses on the remediation and modernization of software Design History Files for an established product family. The primary objective is to improve software and system requirements, close documentation gaps, and rebuild complete end-to-end traceability across requirements, risk controls, software design, implementation, and verification evidence.

Role Overview

GlobalLogic is seeking a skilled DevOps Engineer to join our development team supporting our client. In this role, you will design, maintain, and automate modern CI/CD infrastructure tailored for embedded systems and medical device software. You will work closely with engineering and regulatory teams to ensure that every stage of the software delivery pipeline from static analysis to final build generation is robust, automated, and fully validated in compliance with medical device regulatory standards.

Thanks & Regards

RAJU REDDY |Sr. Team Manager

CIS Technology Inc

Plano, TX 75074

Direct: