CSV Engineer

SummaryWe are looking for a skilled CSV Engineer with strong experience in Veeva systems to support validation, compliance, and implementation activities in a regulated life sciences environment. The ideal candidate will have hands-on experience working on Veeva platforms and ensuring systems meet GxP and 21 CFR Part 11 compliance.Roles & ResponsibilitiesPerform Computer System Validation (CSV) activities for Veeva applications.Develop and execute validation documents: URS, FRS, IQ, OQ, PQ, RTM, etc.Ensure compliance with GxP, 21 CFR Part 11, and regulatory guidelines.Support validation of Veeva Vault, Veeva CRM, or other Veeva applications.Review and approve system changes, patches, and upgrades from a validation perspective.Collaborate with QA, IT, and business stakeholders to maintain validated state.Support audits and inspections by providing validation documentation and evidence.Education & ExperienceStrong experience in Computer System Validation (CSV).Hands-on Veeva experience (Vault / CRM / Clinical / Quality / RIM).Knowledge of GxP, 21 CFR Part 11, and GMP regulations.Experience creating and maintaining validation documentation.Excellent communication and stakeholder management skills.Experience in life sciences or pharmaceutical domain.Exposure to cloud-based system validation.Understanding of SDLC & Agile environments.Seniority levelEntry levelEmployment typeContractJob functionPharmaceutical ManufacturingJ-18808-Ljbffr