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Computer System Validation (CSV) Specialist

Vrinda International

Job Location:

Bengaluru - India

Monthly Salary: L 12 - 14

Experience Required: 4years

Posted: 1 September 2026 (11 hours ago)

Application Deadline: 29 November 2026

Vacancies: 1 Vacancy

Job Summary

HIRING: Computer System Validation (CSV) Specialist

Locations: Hyderabad Bengaluru Chennai Pune

Shift: 12 PM 9 PM

Experience: 48 Years

CTC: 1415 LPA

Domain: CSV GPV GxP

Role Overview

We are looking for an experienced Computer System Validation (CSV) professional with strong exposure to GxP-regulated environments and validation processes. The ideal candidate should have hands-on experience in CSV activities and a good understanding of regulatory compliance and quality systems.

Key Responsibilities

Execute and support Computer System Validation (CSV) activities across the system lifecycle.

Prepare/review validation documentation including URS Risk Assessment IQ/OQ/PQ validation plans and reports.

Ensure compliance with GxP FDA and applicable regulatory requirements.

Support audits deviations CAPA and change-control activities.

Work with cross-functional teams to ensure validated systems remain compliant.

Maintain validation documentation and traceability.

Required Skills

48 years of relevant CSV experience

Strong knowledge of GxP / GMP / regulatory compliance

Experience with CSV lifecycle and validation documentation

Knowledge of risk assessment change control deviation & CAPA

Good communication and stakeholder-management skills

Exposure to GPV / Pharmacovigilance environments is an advantage

Required Skills:

Required Skills 48 years of relevant CSV experience Strong knowledge of GxP / GMP / regulatory compliance Experience with CSV lifecycle and validation documentation Knowledge of risk assessment change control deviation & CAPA Good communication and stakeholder-management skills Exposure to GPV / Pharmacovigilance environments is an advantage

Required Education:

Bachelors Degree (MBA Preferred)

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