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Tier-1 brand, remote role, popular mid-level QA title, and 3–5 year band increase competition.
Regulated CSV/GCP validation experience limits transferability across industries.
Explicit 3–5 years, regulated validation experience, and certification preferences increase screening strictness.
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Validate and lead testing activities for eCOA study software to ensure quality, reliability, and regulatory compliance in clinical trial environments.
Develop, execute, and manage comprehensive test strategies including functional, integration, regression, and performance testing across multiple projects.
Review and approve Computer System Validation (CSV) documentation and lead defect management and cross-functional collaboration to ensure high-quality software releases.
Bachelor’s degree in Information Technology, Computer Science, Software Engineering, or related technical field or equivalent experience.
3 to 5 years of experience in software quality assurance, software testing, or validation.
Experience working in regulated environments such as healthcare, life sciences, medical device, clinical research, or pharmaceutical industries preferred but not strictly mandatory.
Working knowledge of software testing methodologies, SDLC, defect tracking, test management, and Agile development practices.
Experience with Computer System Validation (CSV), Good Clinical Practice (GCP), and audit-ready documentation principles.
Demonstrated ability to lead testing efforts, manage priorities and timelines across multiple projects in regulated healthcare technology environments.
Prepared to mentor junior engineers and contribute to continuous improvement and operational excellence.