Job Summary
We are looking for a Techno‑Functional Consultant with strong experience in Pharmacovigilance (PV) and Veeva Vault Safety. The ideal candidate should have hands‑on PV operations knowledge and the ability to configure, support, and enhance Veeva Safety systems.
Key Responsibilities
Support end‑to‑end Pharmacovigilance activities (case processing, QC, reporting).Configure and maintain Veeva Vault Safety (workflows, objects, fields, permissions, reports).Participate in system upgrades, validation, UAT, and documentation.Liaise with business teams to translate requirements into functional/technical solutions.Provide user support, training, and troubleshooting.Ensure compliance with GxP, SDLC, CSV, and global PV regulations.
Skill Requirements
6–8 years of experience in Pharmacovigilance / Drug Safety.2–3 years hands‑on experience in Veeva Vault Safety.Veeva Platform Certification (mandatory).Strong understanding of ICH, GVP, and global safety regulations.Experience with PV workflows, E2B(R3), and safety system configurations.
Other Requirements
Experience with safety integrations, migrations, or other PV systems (Argus/ARISg).Consulting or life sciences solution delivery background.
EducationBachelor’s/Master’s in Life Sciences, Pharmacy, Biotechnology, B.tech/M.Tech or related field.