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Veeva Vault Regulatory Product Owner

Spadtek Solutions LLCTrenton, NJ🇺🇸United StatesPosted 20 Aug 2026

Quick Overview

Seniority
Mid Senior
Work mode
On Site
Location
Trenton, NJ, United States
Posted
22 hours ago
AgileBusiness AnalysisContinuous ImprovementJiraRequirements GatheringStakeholder Management

Job Description

Job title: Veeva Vault Regulatory Product Owner

Location: Ewing, NJ
Work Arrangement: Hybrid – Onsite 3 days a week
Local Candidates: Required

 

Job Summary

We are seeking a Technical Product Owner to lead the strategy, roadmap, and delivery of digital solutions supporting Product Lifecycle Management (PLM), Quality Management Systems (QMS), and Regulatory processes across global R&D. This role combines product ownership with business analysis, partnering with stakeholders and technical teams to deliver compliant, scalable, and user-focused solutions.

Responsibilities

  • Own the product roadmap, backlog, and delivery priorities for PLM, QMS, and Regulatory platforms.
  • Gather, analyze, and document business requirements, user stories, process flows, and acceptance criteria.
  • Partner with business leaders, IT, and vendors to design, implement, and enhance digital solutions.
  • Support quality and regulatory processes including product lifecycle, change control, CAPA, deviations, audits, complaints, and regulatory documentation.
  • Lead testing activities including SIT, UAT, validation, defect resolution, and production releases.
  • Ensure solutions comply with SDLC, Agile, GxP, FDA 21 CFR Part 11, and Computer System Validation (CSV) requirements.
  • Drive continuous improvement by monitoring adoption, user feedback, and platform performance.

Qualifications

  • Experience as a Product Owner, Business Analyst, or Systems Analyst in a regulated environment.
  • Hands-on experience with Veeva Vault RegulatoryOne, Product Lifecycle Management (PLM), and Quality Management Systems (QMS) is required.
  • Experience supporting regulated R&D, Quality, or Regulatory organizations.
  • Strong understanding of Agile methodologies, backlog management, requirements gathering, and software delivery.
  • Experience with CSV, GxP, FDA 21 CFR Part 11, and validation documentation.
  • Familiarity with Jira, Azure DevOps, ServiceNow, Power BI, Visio, SharePoint, or similar tools.

Preferred Skills

  • Excellent communication and stakeholder management skills.
  • Strong analytical and problem-solving abilities.
  • Ability to translate complex business and regulatory requirements into scalable technical solutions.
  • Experience working with cross-functional teams in fast-paced, highly regulated environments.

 

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