Quality Assurance Team Lead

Bahwan CyberTek; Bengaluru; On-site; INR 800,000 - 1,200,000; Full time

Job summary

A tech solutions provider in Bengaluru seeks a candidate to manage document lifecycle activities in Veeva Vault QualityDocs. Responsibilities include configuring workflows, administering training modules, and ensuring compliance with industry standards. The ideal candidate will collaborate with QA and Regulatory teams, provide training, and drive improvements in processes. Knowledge of GxP and data integrity is essential for this role.

Qualifications

• Experience configuring and supporting Veeva Vault environments for QA/QMS.
• Knowledge of GxP and 21 CFR Part 11 compliance.
• Experience in CSV activities and UAT documentation.

Responsibilities

• Manage document lifecycle activities in Veeva Vault QualityDocs.
• Configure and support workflows, document types, lifecycles, and access controls.
• Administer Veeva Vault Training module with curricula assignment.
• Monitor training compliance, retraining cycles, and generate audit-ready reports.
• Ensure compliance with GxP, 21 CFR Part 11, and data integrity principles.
• Participate in Computer System Validation (CSV) activities including UAT, IQ/OQ/PQ documentation.
• Support change control, document impact assessment, and audit readiness activities.
• Collaborate with QA, Regulatory, IT, and business stakeholders for system enhancements.
• Provide end-user training and resolve system-related queries.
• Drive continuous improvement in QMS documentation and training processes.

Skills

Veeva Vault

GxP compliance

Training management

Education

Bachelor's in Life Sciences

Tools

Quality Management System

Job description

• Manage document lifecycle activities in Veeva Vault QualityDocs (draft, review, approval, effective, obsolete).
• Configure and support workflows, document types, lifecycles, and access controls.
• Administer Veeva Vault Training module including curricula assignment and role-based training matrices.
• Monitor training compliance, retraining cycles, and generate audit-ready reports.
• Ensure compliance with GxP, 21 CFR Part 11, and data integrity principles.
• Participate in Computer System Validation (CSV) activities including UAT, IQ/OQ/PQ documentation.
• Support change control, document impact assessment, and audit readiness activities.
• Collaborate with QA, Regulatory, IT, and business stakeholders for system enhancements.
• Provide end-user training and resolve system-related queries.
• Drive continuous improvement in QMS documentation and training processes.