Veeva Vault - Quality

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)
  
• Strong understanding of FDA, EMA, and GxP regulations
  
• Experience with global or enterprise Vault implementations
  
• Excellent stakeholder communication skills
  

• 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