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A leading global life sciences organization is hiring an Associate Validation Analyst for its Computer System Validation (CSV) team. This hybrid role, based in Bengaluru, is ideal for professionals with 1–2 years of CSV or validation experience in a regulated pharma or clinical environment.
The role focuses on Performance Qualification (PQ), change control, and validated software systems, supporting global stakeholders while working in a second-shift schedule (1 PM – 10 PM IST).
This opportunity is well-suited for candidates aiming to build a long-term career in pharma validation, compliance, and regulated systems support.
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Key Responsibilities – Associate Validation Analyst
- Provide business and system support for validated software systems
- Participate in CSV and PQ validation 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 per SOPs
- Assist in system upgrades, enhancements, and validation testing
- Support users during implementation and post-deployment phases
- Participate in Periodic Reviews to maintain the Master Validation Plan
- Ensure data integrity, testing accuracy, and regulatory compliance
Eligibility & Qualifications
Education
- Bachelor’s degree or equivalent (Science, Pharmacy, IT, or related field)
Experience
- Minimum 1 year of Computer System Validation (CSV) experience – Mandatory
- 1–2 years experience in validation, testing, or regulated environments
Key Skills
- Strong written and verbal communication skills
- Experience with PQ documentation and test execution
- Understanding of pharma regulatory requirements
- High attention to detail and analytical mindset
- Proficiency in MS Word, Excel, and PowerPoint
- Customer-focused, adaptable, and collaborative
Preferred
- Pharma, CRO, or life sciences industry experience
- Exposure to regulated software systems
Work Schedule & Location
- Work Mode: Hybrid
- Shift Timing: 1:00 PM – 10:00 PM IST
- Locations:
- Bengaluru, India
- Taguig City, Philippines
Salary & Benefits
- Estimated Salary (India): ₹4,00,000 – ₹7,00,000 per annum
- Hybrid working model
- Global exposure in regulated systems
- Structured learning in CSV and validation lifecycle
- Career growth in pharma compliance and quality systems
(Salary may vary based on experience and interview performance)
How to Apply
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