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Tier-1 employer, metro location, broad DevOps skillset and a generic DevOps title raise competition density.
Requires healthcare regulatory and medical device compliance experience, making background fit highly industry-specific.
Explicit 10+ years plus regulatory, Azure DevOps, and automation mandates create strict shortlisting filters.
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Lead standardization and automation of DevOps practices to improve development, delivery, deployment, and operational workflows.
Build and maintain end-to-end automation frameworks and CI/CD pipelines to drive high productivity.
Collaborate with Engineering teams and senior architects to evaluate feasibility and implement scalable DevOps solutions across enterprise systems including desktop, web, mobile, and medical devices.
10+ years of total product development experience with 5 to 8 years specifically in Automation and DevOps.
Bachelor’s or Master’s degree in Engineering or Technology (Computer Science, Computer Engineering, Electronics, Electricals, or related).
Experience with healthcare regulatory standards such as FDA and ISO (IEC 62304) and Non-Product Tool Validation as per FDA Medical standards.
Hands-on expertise in Azure DevOps administration, Azure DevOps Services REST API, CI/CD pipelines, Python programming, Git (branching strategies, repo management), database management (MS SQL), and Agile methodology.
Experienced in healthcare or medical device software development environments requiring compliance with FDA and ISO standards.
Strong technical leadership skills with ability to influence cross-disciplinary teams including R&D, product design, and operations.
Demonstrated ability to manage large-scale enterprise automation frameworks integrating various tools (e.g., Jenkins, Ansible, Postman) and cloud/hybrid-cloud environments.