Veeva Vault - Quality
Job description
Job Description 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, strong analytical skills, and the ability to translate complex technical and compliance requirements into clear, client-ready solutions.
Key Responsibilities
Hands on experience with end-to-end implementation of Veeva Vault Quality modules (QMS, Training, eTMF, Quality. Docs) 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 Required Qualifications 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 Mandatory Certifications Required: Veeva Vault Quality Suite (QMS, eTMF, Training, Docs, etc.)
Benefits Perks & Benefits Permanent work-from-home Flexi Week culture (5 days / Alternate 4-day work week) Fixed internet allowance Other benefits
Description copied from P360's careers page. Read the full posting before you apply.
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