Veeva Quality Docs Engineer

3 days ago

Hyderabad, Telangana, India Technogen Full time ₹ 15,00,000 - ₹ 25,00,000 per year

Job Summary:

We are looking for an experienced Veeva Vault QualityDocs Engineer to join our Life Sciences technology team. The ideal candidate will have strong expertise in Veeva Vault QualityDocs configuration, customization, and integration, ensuring seamless document management and compliance with regulatory requirements. This role involves working closely with QA, IT, and business stakeholders to deliver high-quality solutions in a regulated environment.

Key Responsibilities:

  • Configure, customize, and maintain Veeva Vault QualityDocs applications.
  • Collaborate with business and QA teams to gather requirements and implement solutions.
  • Develop and manage workflows, document lifecycles, user roles, and permissions.
  • Support validation activities (IQ/OQ/PQ) and author related documentation.
  • Troubleshoot and resolve issues in QualityDocs environments.
  • Ensure compliance with GxP, FDA 21 CFR Part 11, and other regulatory standards.
  • Train and support end-users on system usage and best practices.
  • Participate in upgrades, patches, release management, and system enhancements.
  • Maintain documentation including SOPs, technical specifications, and configurations.

Required Skills & Qualifications:

  • 68 years of overall IT experience with 3–5 years in Veeva Vault QualityDocs.
  • Strong understanding of document management systems in the pharmaceutical/life sciences domain.
  • Hands-on experience in Vault configuration, workflows, lifecycle management.
  • Good knowledge of GxP compliance, validation, and regulatory documentation.
  • Strong problem-solving, communication, and stakeholder engagement skills.
  • Ability to work independently in a remote setup and within cross-functional teams.
  • Veeva Vault certification preferred.
  • Experience with Agile/Scrum methodologies desirable.

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