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Tier-1 brand and metro location increase applicants, but senior specialized SDET requirements reduce competition.
GxP/CSV regulatory and biotech-specific validation requirements limit cross-industry transferability.
Explicit 12–17 years, CSV/GxP regulatory expertise, and automation leadership create strict filtering criteria.
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Lead design, development, and evolution of enterprise-wide Quality Engineering and Test Automation frameworks for AI, intelligent automation, and AI-native applications.
Define and implement scalable automation frameworks, modern testing strategies, and engineering best practices across complex enterprise software solutions.
Collaborate with engineers, architects, DevOps, and product teams to ensure high-quality, compliant, and resilient software delivery, including support for Computer System Validation (CSV) in regulated environments.
12-17 years of experience in Business, Engineering, IT, or related field.
Strong expertise in software engineering with languages like Java, Python, JavaScript/TypeScript, or C# and proven experience building enterprise-scale test automation frameworks.
Deep knowledge of Quality Engineering and Test Automation tools such as Selenium, Playwright, UiPath Test Suite, Postman, and experience with CI/CD tools like Jenkins, GitHub Actions, Azure DevOps.
Experience with Computer System Validation (CSV), GxP compliance, FDA 21 CFR Part 11, EU Annex 11 regulations in software validation.
Technical leadership experience driving Quality Engineering strategies and establishing automation standards across Agile and DevSecOps teams.
Expertise in cloud-native application testing, microservices, distributed systems, and modern DevOps toolchains.
Experience mentoring engineers on automation frameworks and modern Quality Engineering methodologies in regulated enterprise environments.