Veeva Vault Quality Technical Lead
Job in
Indiana Borough, Indiana County, Pennsylvania, 15705, USA
Listed on 2026-08-18
Listing for:
United Pharma Technologies Inc
Full Time
position Listed on 2026-08-18
Job specializations:
-
Quality Assurance - QA/QC
IT QA Tester / Automation, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
Senior Veeva Vault Quality Technical Lead
Location:
Indianapolis, IN
Position Overview
We are seeking a Senior Veeva Vault Quality Technical Lead to serve as the technical authority for the Veeva Vault Quality platform and support strategic digital Quality initiatives. This role will partner closely with Product Management, Architecture, Integration, Data, and business teams to design and deliver complex Veeva Quality solutions within a regulated GxP environment.
Key Responsibilities
- Serve as the technical lead for Veeva Vault Quality, supporting strategic platform enhancements and business initiatives.
- Design, configure, test, and deploy complex Veeva Vault QMS and Quality Docs (QDocs) solutions.
- Configure and manage document life cycles, workflows, security models, objects, and related platform capabilities.
- Support Quality processes including Deviations, CAPA, Change Control, Quality Events, Controlled Documents, and Training.
- Provide technical leadership and escalation support to managed service providers, implementation partners, and support teams.
- Support CSV/validation, release management, change control, and compliance activities in regulated GxP environments.
- Collaborate with architecture, integration, and data teams to support integrations between Veeva Vault Quality and enterprise platforms.
- Drive continuous improvement and technical solutions that align with the organization's digital Quality strategy.
Required Qualifications
- Bachelor's degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.
- 7+ years of experience supporting regulated GxP systems.
- 5+ years of Veeva Quality Vault experience.
- 3+ years of hands-on Veeva Vault Quality configuration experience.
- Strong experience with Workflows, Life cycles, Security Models, Objects, and Quality Docs.
- Proven experience delivering complex platform enhancements and Quality business process improvements.
- Pharmaceutical, biotechnology, or other life sciences industry experience.
- Strong understanding of GxP requirements, validation, change control, and regulated system environments.
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