Principle DevOps Engineer; Medical Devices & Embedded Systems) IRC

Function IT, Telecom & Internet

Experience 10-15 years

Location United States - Waltham MA

Skills CI/CD Tools, Dev Ops, Healthcare-Medical Devices

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

Global Logic is seeking a skilled Dev Ops 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

Global Logic 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.

Global Logic 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.

• Minimum of 10 years of experience in Dev Ops 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 Dev Sec Ops  tools (e.g., Sonar Qube, Black Duck SCA, Artifactory, Git Hub Enterprise, and Jenkins) embedded within deployment workflows.
• Dev Ops Expertise:
  Strong experience setting up and managing CI/CD tools (e.g., Jenkins, Git Lab CI, Git Hub Actions, or Azure Dev Ops).
• Embedded Software Build Environments:
  Hands-on experience with build automation tools (e.g., CMake, Make, Docker, GCC/Clang tool chains) for embedded or hardware-centric systems.
• Quality Tools Integration:
  Experience integrating static analysis tools (e.g., Sonar Qube, 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 Power Shell for build and task automation.

• CI/CD Pipeline Management:
  Architect, optimize, and manage continuous integration and deployment (CI/CD) pipelines and developer tool chains.
• 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…