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Argus/IVP Tester in PV Job Opening at IQVIA

Published on

IQVIA

1 - 4 Years

Bangalore

B.Pharm/M.Pharm/Pharm.D/MSc/BSc/Life Sciences graduates are eligible

Verified Job

Online Application

Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions for the life sciences industry. We provide intelligent insights to accelerate medical innovations and improve patient outcomes worldwide. With cutting-edge technology and deep industry expertise, IQVIA helps pharmaceutical, biotech, and healthcare organizations navigate complex regulatory landscapes and deliver life-changing therapies.


Argus/IVP Tester – Key Responsibilities

1. Test Planning & Design

  • Develop detailed test plans, scenarios, and scripts for Oracle Argus & IVP (Intake Validation Platform).
  • Create Validation Test Protocols (VTPL) and User Acceptance Test (UAT) plans.
  • Collaborate with business analysts to align testing with functional requirements.

2. Test Execution

  • Perform end-to-end testing of data migration between Argus & IVP.
  • Validate data accuracy, transformations, and interface functionality.
  • Log, track, and resolve defects with detailed documentation.

3. Documentation & Compliance

  • Prepare Standard Operating Procedures (SOPs) and Test Execution Reports.
  • Ensure compliance with GxP, FDA 21 CFR Part 11, and other regulatory standards.
  • Support audits by providing testing evidence and validation documents.

4. Collaboration & Continuous Improvement

  • Work with developers, business analysts, and stakeholders to optimize system performance.
  • Support change management for Argus configurations and IVP updates.
  • Identify process improvements to enhance testing efficiency.

Qualifications & Skills

✅ Experience in Oracle Argus Safety & IVP testing.
✅ Strong knowledge of data migration, validation, and regulatory compliance.
✅ Proficiency in test case design, defect tracking, and reporting.
✅ Familiarity with GxP, FDA 21 CFR Part 11, and pharmacovigilance processes.
✅ Excellent communication & collaboration skills.

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How to Apply

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