Associate Software Quality & Test Analyst
Aufgaben
- Support system validation and qualification activities for software applications used in regulated business environments.
- Develop, review, and execute test cases, test scripts, and user acceptance testing (UAT) scenarios to verify system functionality and compliance with requirements.
- Prepare, review, and maintain validation documentation, quality records, and supporting evidence in accordance with established procedures.
- Assist with change request assessments, testing activities, implementation planning, and change control documentation.
- Record test results, identify and document defects, and maintain clear evidence of testing activities and outcomes.
- Ensure traceability between business and system requirements, test cases, results, and validation deliverables.
- Support audit and inspection readiness by keeping documentation accurate, complete, organized, and readily accessible.
- Collaborate with business stakeholders, IT teams, Quality professionals, and external vendors to support system improvements and project delivery.
- Follow established quality procedures and contribute to continuous improvement in testing, validation, and compliance practices.
Anforderungen
- Bachelor's degree in Information Technology, Computer Science, Life Sciences, Engineering, or a related discipline.
- One to three years of experience in software testing, quality assurance, system validation, or a related role.
- Understanding of the Software Development Life Cycle (SDLC), software testing methodologies, test documentation, and user acceptance testing processes.
- Strong analytical and problem-solving abilities, with excellent attention to detail and a commitment to documentation accuracy.
- Good written and verbal communication skills, including the ability to explain testing outcomes and collaborate effectively with cross-functional teams.
- Familiarity with defect tracking, change management, and quality management processes.
- Ability to manage assigned tasks, follow established procedures, and maintain clear records in a structured, compliance-focused environment.
- Preferred: Experience with Computer System Validation (CSV) and familiarity with regulated life sciences or clinical research environments.
- Preferred: Knowledge of Good Practice (GxP) principles, GAMP 5 guidance, and FDA 21 CFR Part 11 requirements relating to electronic records and electronic signatures.
- Preferred: Experience with tools such as Jira, ServiceNow, HP ALM, or similar platforms used for testing, issue tracking, and quality management.
Wir bieten
- Remote work opportunities across multiple locations in India, including Bengaluru, Hyderabad, Chandigarh, Noida, and Mohali.
- Full-time employment within a collaborative, growth-oriented environment.
- Opportunities to develop skills in software quality assurance, system validation, testing, and regulatory compliance.
- Exposure to cross-functional projects involving business, IT, Quality, and external stakeholders.
- Professional development opportunities to support long-term career growth in life sciences technology and clinical research.
- The opportunity to contribute to data integrity, system reliability, and quality practices that support patient-focused research.
- Salary, healthcare coverage, and additional benefits: Specific details were not provided in the source job description and should be confirmed during the recruitment process.
Bewerbung
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Sonstiges
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