We're seeking an experienced Developer - Vault Quality to design, implement, and optimize Veeva Vault Quality (QMS) solutions in regulated life sciences (GxP) environments. The ideal candidate has hands-on experience with Vault QMS, CSV/Validation, and regulated documentation, solid analytical skills, and the ability to translate complex technical and compliance requirements into clear, client-ready solutions.

Responsibilities

- Hands on experience with end-to-end implementation of Veeva Vault Quality modules (QMS, Training, eTMF, QualityDocs)
- Act as functional SME for GxP processes (Deviations, CAPA, Change Control, Audits)
- Drive business workshops, requirements gathering, and solution design
- Configure Vault Quality objects, workflows, lifecycle states, and security
- Partner with validation, IT, and business stakeholders to ensure compliance
- Support UAT, go-live,



and post-production hypercare

Requirements

- 5 years of hands-on Veeva Vault Quality experience
- Active Veeva Vault Quality certification(s) (mandatory)
- Strong understanding of FDA, EMA, and GxP regulations
- Experience with global or enterprise Vault implementations
- Excellent stakeholder communication skills

Qualifications

- Mandatory certifications required: Veeva Vault Quality Suite (QMS, eTMF, Training, Docs, etc.)

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.

📌 Veeva Vault - Quality Professional (India)
🏢 P360
📍 India