Greetings from P360..
About us:
P360 is an advanced pharma software company specializing in business technology development and implementation for pharmaceutical and life sciences companies worldwide. We specialize in technology that boosts operational efficiency across the entire organization while giving a unique view of how your internal process is functioning and how to improve them.
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, 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
Required Qualifications
5 years of hands-on Veeva Vault Quality experience
Active Veeva Vault Quality certification(s) (mandatory)
Robust 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.)
Perks & Benefits
Permanent work-from-home
Flexi Week culture (5 days / Alternate 4-day work week)
Fixed internet allowance
Other benefits
Note: We will contact candidates who fit the current requirements. If you are not contacted, your information and resume will be kept in our database, so w
📌 Veeva Vault Quality | Remote (India)
🏢 P360
📍 India