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Posted 13 Oct 2025

Veeva QMS developer

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Team
Cyient
Posted
13 Oct 2025

About the role

Job Title: Veeva QMS Developer

Location: Bengaluru, India

Experience: 5+ Years

Job Type: Full-Time (On-site / Hybrid / Remote – as per company policy)

Department: IT / Quality Systems Development

Industry: Life Sciences / Pharmaceuticals / IT Services

Job Summary:

We are seeking a highly skilled and motivated Veeva QMS Developer with 5+ years of experience to join our team in Bengaluru. The ideal candidate will have in-depth experience in configuring, customizing, and maintaining the Veeva Vault Quality Suite, including modules such as Document Control, Change Control, CAPA, Audit Management, and Training. This role requires strong technical and domain expertise in Life Sciences and GxP-compliant systems.

Key Responsibilities:
  • Design, configure, and implement solutions in Veeva Vault QMS, based on business requirements.
  • Develop and maintain workflows, object lifecycles, reports, and custom configurations within Veeva Vault.
  • Collaborate with business analysts, QA, and project managers to gather and understand functional requirements.
  • Support system integration activities between Veeva and other enterprise systems (ERP, LMS, etc.).
  • Manage and troubleshoot Vault configuration issues and enhancements.
  • Participate in validation activities (CSV), including creation of IQ, OQ, PQ protocols.
  • Ensure solutions adhere to compliance requirements (21 CFR Part 11, GxP, GDPR).
  • Support change management, deployments, and user acceptance testing (UAT).
  • Provide technical documentation, training, and user support for Veeva applications.
  • Stay current with new Veeva releases and features, and recommend optimizations.
Required Skills & Qualifications:
  • Bachelor’s degree in Computer Science, Information Technology, or a related field.
  • Minimum 5 years of experience working in IT, with at least 2–3 years specifically on Veeva Vault QMS development.
  • Hands-on experience configuring Veeva Vault objects, lifecycles, workflows, and reports.
  • Good understanding of quality processes in regulated industries (Life Sciences, Pharma).
  • Strong knowledge of GxP, 21 CFR Part 11, Annex 11, and other regulatory frameworks.
  • Experience with system integration tools (REST APIs, middleware, etc.).
  • Ability to translate business needs into scalable Veeva Vault solutions.
  • Strong analytical and problem-solving skills.
  • Excellent written and verbal communication skills.
Preferred Skills (Good to Have):
  • Veeva Vault QMS certification (Developer/Admin).
  • Experience with VQL (Veeva Query Language) and Veeva API.
  • Experience with Agile/Scrum methodologies.
  • Exposure to other Vault applications like Veeva QualityDocs or RIM.
  • Prior experience working with global teams.
Benefits:
  • Competitive salary and performance incentives
  • Health and wellness benefits
  • Learning & development opportunities (including Veeva certifications)
  • Work-life balance and flexible work options
  • Opportunity to work on global regulatory projects

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