Job description

Description 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. Note GlobalLogic estimates the starting pay range for this role to be performed in Waltham, MA to be $140K to $150K and reflects base salary only and does not include additional performance-linked variable compensation, benefits etc. that may be applicable for the role. This pay range is provided as a good faith estimate and the amount offered may be higher or lower. GlobalLogic takes many factors into consideration in making an offer, including candidate qualifications, work experience, operational needs, travel and onsite requirements, internal peer equity, prevailing wage, responsibilities, and other market and business considerations. Requirements • Minimum of 10 years of experience in DevOps including hands-on experience building and managing cloud environments for regulated medical devices, healthcare, diagnostics, or similarly controlled environments. • 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, linetrs, 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. What we offer Exciting Projects: Come take your place at the forefront of digital transformation! With clients across all industries and sectors, we offer an opportunity to work on market-defining products using the latest technologies. Collaborative Environment: You can expand your skills by collaborating with a diverse team of highly talented people in an open, laidback environment — or even abroad in one of our global centers or client facilities! Work-Life Balance: GlobalLogic prioritizes work-life balance, which is why we offer flexible work schedules and opportunities to work from home. Professional Development: We provide continuing education classes, professional certification and training (technical, soft skills, language, and communication skills) to help you realize your professional goals. Being part of a global organization, there are additional learning opportunities through international knowledge exchanges. Excellent Benefits: We provide our employees with competitive salaries, health and life insurance, short-term and long-term disability insurance, a matched contribution 401K plan, flexible spending accounts, and PTO and holidays About GlobalLogic GlobalLogic, a Hitachi Group Company, is a trusted digital engineering partner to the world’s largest and most forward-thinking companies. Since 2000, we’ve been at the forefront of the digital revolution – helping create some of the most innovative and widely used digital products and experiences. Today we continue to collaborate with clients in transforming businesses and redefining industries through intelligent products, platforms, and services.

Requirements

Must-haves

The customer is a global medical device company developing point-of-care diagnostic systems used in hospital and clinical environments.
Minimum of 10 years of experience in DevOps including hands-on experience building and managing cloud environments for regulated medical devices, healthcare, diagnostics, or similarly controlled environments.
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.
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, linetrs, 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.

Nice-to-haves

None flagged.

Application prep

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Keywords to mirror

ci/cdazuredockerpython

Platform: globallogic
Effort: medium

Benefits

Benefits detected in the listing.

401k

Pto

Professional Development