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Metro location and broad QA responsibilities increase candidate density despite lower company brand.
Clinical validation and regulated QA work reduces cross-industry transferability significantly.
Regulated clinical validation and audit responsibilities imply stringent compliance and domain-specific hiring filters.
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Define and create detailed test cases and scripts for functional and non-functional software quality aspects, ensuring traceability to requirements.
Monitor, analyze, and report on test execution, results, defect tracking, and overall system quality during the software development lifecycle.
Conduct audits for compliance, manage stakeholder communications, and contribute to continuous improvement of test methods, tooling, and problem resolution processes.
Work Experience Required: Not explicitly mentioned in the JD.
Mandatory Skills: Expertise in software quality testing including creation of test scripts, test data specification, regression testing, defect management, and quality assurance audits.
Communication: Excellent verbal and written communication skills required to present complex information to diverse audiences.
No explicit degree, location, or notice period requirements mentioned.
Experienced in both functional and non-functional software testing within regulated environments related to clinical or biopharmaceutical software preferred but not explicitly required.
Able to work collaboratively with diverse stakeholders including customers, suppliers, and technical teams to ensure user needs are met and software quality is optimized.
Skilled in applying and improving testing standards, tools, and methods with a focus on continuous quality improvement and compliance.