Associate Validation Analyst

Roles & Responsibilities
• Provide business and system support for validated software systems
• Participate in Computer System Validation (CSV) and Performance Qualification (PQ) activities across the SDLC
• Prepare and review Validation Plans, PQ Test Cases, and Validation Summary Reports
• Author, execute, and document PQ test scripts with complete compliance evidence
• Review and support Change Control documentation in line with SOPs
• Assist in system upgrades, enhancements, and related validation testing
• Support users during system implementation and post-deployment phases
• Participate in Periodic Reviews to maintain the Master Validation Plan
• Ensure data integrity, testing accuracy, and regulatory compliance

Qualification
• Bachelor’s degree in Science, Pharmacy, IT, or related discipline

Experience
• Minimum 1 year of Computer System Validation (CSV) experience (mandatory)
• 1–2 years of experience in validation, testing, or regulated environments

Skills
• Strong written and verbal communication skills
• Hands-on experience with PQ documentation and test execution
• Understanding of pharmaceutical regulatory requirements
• High attention to detail and strong analytical mindset
• Proficiency in MS Word, Excel, and PowerPoint
• Customer-focused, adaptable, and collaborative working style
• Experience in pharma, CRO, or life sciences industry
• Exposure to regulated and validated software systems

About the Organization
A leading global life sciences organization supporting regulated pharmaceutical and clinical systems through robust validation, compliance, and quality-driven technology solutions. The organization works closely with global stakeholders to ensure system reliability, data integrity, and regulatory readiness.