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Veeva Regulatory Business Analyst || Princeton, New Jersey(Hybrid)

Verito SolutionsPrinceton, NJ🇺🇸United StatesPosted 7 Jul 2026

Quick Overview

Work Type
On Site
Level
Mid Senior

Job Description

Veeva Regulatory Business Analyst

 Princeton, New Jersey(Hybrid)

12+ month contract 

 

Please ensure each candidate can produce a manager or director level reference

looking for a Veeva Regulatory BA to own and evolve the digital and AI product capabilities that support product lifecycle management, quality management, and regulatory business processes across global R&D. This will be a 12+ month contract onsite in the Princeton, NJ area - in-office 3 days per week.

Job Description

 

The individual will serve as a key liaison between business stakeholders, technical teams, vendors, and governance partners to deliver compliant, user-centered, inspection-ready solutions that improve process efficiency, data quality, and cross-functional visibility.

Experience

  • 7+ years of experience in product ownership, business analysis, systems analysis, or technology delivery within regulated environments.
  • Experience supporting PLM, QMS, Regulatory Information Management, document management, workflow, or enterprise quality/regulatory platforms. Must have hands on experience with Veeva Vault RegulatoryOne, Product Lifecycle Management and Quality Management Systems.
  • Strong understanding of product development, specification management, change control, quality events, CAPA, audits, complaints, submissions, registrations, claims, or regulatory documentation processes.
  • Experience working with cross-functional teams across R&D, Quality, Regulatory, Operations, IT, and external vendors.
  • Experience supporting validated systems, inspections, audits, and regulated technology delivery preferred.

Technical Skills

  • Strong knowledge of Agile, hybrid delivery, SDLC, backlog management, user story writing, acceptance criteria, and release planning.
  • Hands-on experience documenting business requirements, process maps, workflows, data flows, test cases, validation artifacts, and traceability matrices.
  • Working knowledge of GxP, FDA 21 CFR Part 11, EU Annex 11, data integrity, audit trails, electronic records/signatures, and change control expectations.
  • Familiarity with PLM, QMS, RIM, document management, reporting, analytics, integration, and workflow automation tools.
  • Experience with tools such as Jira, Azure DevOps, ServiceNow, Power BI, Visio, Miro, SharePoint, or similar platforms.
  • roject:
    • Must Have: Veeva
    • Must Have: Regulatory  (does not have to be an expert in regulations)
  • Regulatory Information Management System with Veeva
    • Bolt on module (lower level from Veeva)
    • 50 global users
  • Business Analyst that has a regulatory (Veeva Specific) background – No current expertise on team with Regulatory/Veeva background
    • Needs someone who really knows the system
    • Work with vendor to implement and integrate
    • Roll up sleeves and get dirty
    • Thinking someone 10 years in as a BA, growing into a Product Owner
  • Long term vision for the role would be to turn this into a product owner, will own the Regulatory, Veeva, QMS tracks
  • Needs leadership experience, but person has to be in the weeds on project
  • Veeva will be doing the implementation themselves
 
 
(“ Believe you can and you’re halfway there. ”)
 –  Theodore Roosevelt
Sayantan Das   Senior  Tech Recruiter
E: 
P: +1  |

Skills

Agile
Business Analysis
Jira
Miro

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