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Tier-1 brand, remote role, common QA title, and early-mid experience attract many qualified applicants.
Core QA skills transfer broadly, but CSV and regulated clinical context increase industry specificity to medium.
Explicit 1–3 years requirement plus preferred certifications and regulated-experience preference create moderate shortlisting strictness.
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Own validation and testing activities for assigned eCOA study software projects ensuring compliance with SOPs and regulatory standards.
Design, execute, and document various testing types including functional, integration, regression, and performance testing with traceability to requirements.
Manage testing timelines, communicate status, risk, and escalate issues while collaborating with cross-functional and global teams to drive quality outcomes.
Bachelor’s degree in IT, Computer Science, Software Engineering, or related field, or equivalent practical experience.
1 to 3 years of software testing, quality assurance, or validation experience.
Knowledge of software development lifecycle, testing principles, test design and execution, validation practices, and defect management.
Work Experience Required: 1 to 3 years in software testing or quality assurance in regulated or similar environments.
Experienced in regulated environments such as healthcare, life sciences, clinical research, medical devices, or pharmaceuticals.
Familiar with Computer System Validation (CSV), Good Clinical Practice (GCP), audit-ready documentation, and Agile development methodologies.
Capable of independently managing multiple priorities, and coordinating with global and offshore teams, with strong analytical skills and attention to detail.