
10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
đ„ 2 minutes ago
đźđł India â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§ QA Engineer (Quality Assurance)
đ» Ghost score 10%
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10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
âą Support system validation and qualification activities for software applications âą Develop and execute test cases, test scripts, and user acceptance testing (UAT) scenarios âą Create, review, and maintain validation and quality documentation âą Support change request assessment, testing, and implementation activities âą Document test results, defects, and testing evidence âą Ensure traceability between requirements, testing, and validation deliverables âą Assist with audit readiness by maintaining accurate and inspection-ready records âą Collaborate with business, IT, Quality, and vendor teams on system enhancements and projects âą Contribute to software quality, system validation, testing, and compliance activities for regulated business applications
âą Bachelor's degree in information technology, Computer Science, Life Sciences, Engineering, or a related field âą 1-3 years of experience in software testing, validation, quality assurance, or related roles âą Understanding of the Software Development Life Cycle (SDLC), software testing methodologies, and user acceptance testing (UAT) processes âą Strong analytical, documentation, and problem-solving skills âą Excellent verbal and written communication skills âą Strengths in software testing and UAT, system validation, and quality documentation âą Understanding of regulated environments and related documentation and compliance standards âą Ability to collaborate across teams and communicate clearly âą Patient-focused mindset and strong attention to detail âą Comfort working with change management and defect tracking processes âą Preferred: Experience with Computer System Validation (CSV) âą Preferred: Knowledge of Good Practice (GxP), Good Automated Manufacturing Practice (GAMP 5), and FDA 21 CFR Part 11 requirements âą Preferred: Experience with change control and quality management processes âą Preferred: Familiarity with Jira, ServiceNow, HP ALM, and similar tools
âą Flexible work arrangements âą Growth opportunities âą Continuous learning opportunities âą Career paths and skill expansion across clinical research
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â° Full Time
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đ§ QA Engineer (Quality Assurance)
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