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Tier-1 employer, generic QA title, and remote flexibility increase applicant competition.
Core QA skills transfer broadly but CSV and life‑sciences validation requirements increase industry specificity.
Explicit 1–3 years plus regulatory and tooling preferences create moderate candidate filtering.
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Own validation and testing of eCOA study software ensuring compliance with Computer System Validation (CSV) SOPs.
Manage and execute testing activities including functional, integration, regression, and performance tests across multiple projects with traceability to requirements.
Collaborate with cross-functional and global teams to remove roadblocks, monitor timelines, report status, and ensure software meets regulatory, business, and customer expectations.
Bachelor’s degree in IT, Computer Science, Software Engineering or related technical field (or equivalent experience).
1 to 3 years of software testing, quality assurance, or validation experience.
Knowledge of software development lifecycle (SDLC), validation practices, and software testing principles including defect management and requirements traceability.
Work Experience Required: 1 to 3 years in testing/validation
Experience working in regulated environments like healthcare, life sciences, clinical research, or pharmaceutical industries is preferred and beneficial for compliance understanding.
Familiarity with Computer System Validation (CSV), Good Clinical Practice (GCP), and audit-ready documentation is advantageous for success.
Comfortable working with defect tracking, test management tools, and collaborating with global/offshore teams following Agile and modern software delivery practices.
