CSV Team member - Contract
SSS Grameen Services · Ahmedabad · onsite · Posted 63d ago
Undisclosed8–13 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Job Summary
8+ years of experience in Computer System Validation (CSV) within the pharmaceutical or life sciences industry. Strong knowledge of GxP regulations, FDA requirements, and industry compliance standards governing validated systems.
Responsibilities
- Proven experience in preparing, reviewing, and approving validation deliverables, including Validation Plans, Risk Assessments, URS, FS, Traceability Matrix, Test Scripts, IQ/OQ/PQ, SIT, UAT, and Validation Summary Reports.
- Expertise in ensuring regulatory compliance, audit readiness, data integrity, and system validation throughout the project lifecycle.
- Capable of supporting validation strategy, testing execution, compliance reviews, defect management, document signoffs, go-live readiness, and hyper care support for SAP implementations in a regulated environment.
Contract Details
- Job Type: Contract
- Location: Ahmedabad, Gujarat, India
- Period: 6-12 months
Job Opening Name
(Ref:BM) CSV Team member - Contract (Work from Office Ahmedabad)
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
data integritySAPAudit ComplianceTest scriptsComputer System ValidationDefect managementRegulatory CompliancecompliancePharmaLife Sciences