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Zimmer Biomet Holdings

Develops joint replacement, robotics, smart implants

Senior Devops & Release Engineer

DevOps EngineeringUpdated on Nov 9
Full-timeSalt Lake City, UT, USANo salary listed

About the Job

Requirements

  • At least 6 years of experience in DevOps, Release Engineering, or System Engineering.
  • Deep Linux administration experience, preferably in Debian or Ubuntu environments.
  • Experience with bare-metal and on-premise systems.
  • Programming experience with Python, Bash, and C++.
  • Strong understanding of system security, networking, deployment architectures, and operational best practices.
  • Experience with GitHub administration, continuous integration and continuous delivery (CI/CD) tooling, Jira, and source control governance.
  • Hands-on experience with Jenkins, TeamCity, or similar CI platforms.
  • Experience supporting GPU-enabled systems and native application build environments.
  • Experience with AWS and Azure cloud ecosystems.

Responsibilities

  • Design, implement, and maintain secure and reproducible DevOps infrastructure supporting Linux-based medical software and hardware.
  • Own the end-to-end software build, packaging, release, deployment, and operational lifecycle while ensuring compliance with FDA, ISO 13485, IEC 62304, and ISO 14971 expectations.
  • Implement scalable automation, secure deployment mechanisms, validated CI/CD systems, and traceable release processes appropriate for regulated environments and audit readiness.
  • Administer Debian Linux systems.
  • Support Linux-based deployment and security on bare-metal devices, not cloud.
  • Design, maintain, and evolve DevOps and release engineering platforms.
  • Ensure reliability, reproducibility, and operational consistency across development, validation, testing, and production systems.
  • Align operational practices with risk management and post-market surveillance activities.
  • Own software build, packaging, release, rollback, and patch management processes.
  • Support controlled software release strategies consistent with regulated medical environments.
  • Design and maintain CI/CD pipelines supporting regulated software development workflows.
  • Administer and optimize tooling including GitHub, Jenkins, TeamCity, or equivalent systems.
  • Automate build generation, testing, static analysis, packaging, and artifact management.
  • Ensure CI/CD outputs are auditable and suitable as objective evidence during inspections and audits.
  • Ensure infrastructure and DevOps practices comply with IEC 62304, ISO 13485, ISO 14971, and FDA cybersecurity guidance.
  • Implement defense-in-depth security controls across build systems, deployment pipelines, and operational environments.
  • Enforce least-privilege access, authentication controls, secure secrets management, and audit logging.
  • Support internal audits, FDA inspections, and ISO certification activities through documentation and evidence generation.
  • Support lifecycle management of ML/AI inference components within regulated environments.
  • Ensure model versioning, traceability, controlled promotion, and alignment with released software versions.
  • Maintain reproducible ML build environments and containerized workflows where appropriate.
  • Implement monitoring, logging, and operational observability for on-premise clinical systems and development environments.
  • Support incident response, root cause investigations, CAPAs, and continuous improvement initiatives.
  • Maintain operational records and deployment logs supporting audit and compliance requirements.
  • Act as the primary technical authority for DevOps and release engineering practices.
  • Mentor junior DevOps and platform engineers.
  • Translate regulatory and quality requirements into practical, scalable technical implementations.
  • Maintain operational documentation, deployment procedures, rollback guides, and technical runbooks.

Desired Qualifications

  • Experience with C++ and QT-based applications.
  • Experience working in regulated industries such as medical devices, healthcare, or life sciences.
  • Familiarity with IEC 62304, ISO 13485, and ISO 14971 standards.
  • Experience supporting validation activities, audits, inspections, and compliance evidence generation.
  • Prior experience supporting Software as a Medical Device (SaMD) products.
  • Experience with ML/AI deployment workflows in regulated environments.
  • Experience designing DevOps systems intended for regulatory evidence and audit readiness.

About the Company

Zimmer Biomet Holdings

Develops joint replacement, robotics, smart implants

Zimmer Biomet manufactures and markets musculoskeletal medical devices and instruments for joint replacement, surgical trauma, and sports medicine. Its products include joint implants, surgical tools, and smart implants, often supported by robotic-assisted surgery systems. The company develops, produces, and sells these devices and provides services such as medical education and training to healthcare professionals to support procedures and outcomes. Compared with competitors, Zimmer Biomet benefits from a long history (over 90 years), a global footprint, and a focus on integrated solutions that combine advanced implants with robotics technology and education partnerships. Its goal is to advance patient care by delivering reliable devices, technologies, and professional training that improve surgical outcomes and collaboration with healthcare providers.

Company size
10,001+
Company stage
IPO
Headquarters
Warsaw, IN
Founded
1927

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