Senior Business Analyst

Karwell Technologies

  • Warren, NJ
  • 12 days ago
  • Instant Apply
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Skills

  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Business Analysisunmatched
  • Business Supportunmatched
  • Code of Federal Regulationsunmatched
  • Communication Skillsunmatched
  • Design Documentunmatched
  • Functional Testingunmatched
  • GxPunmatched
  • Insurance Regulationsunmatched
  • Presentation/Verbal Skillsunmatched
  • Quality Assuranceunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Requirements Managementunmatched
  • Use Casesunmatched
  • Writing Skillsunmatched

Description

Job Summary:
  • We are seeking a Senior Business Analyst Veeva Vault Quality to support Business & Technology Integration for Veeva Quality Docs/QMS implementation within the Life Sciences domain.
  • The role is responsible for gathering business requirements, creating user stories, designing workflows, ensuring CSV alignment, and serving as the liaison between Business and IT teams in a GxP-regulated environment.
Roles & Responsibilities:
  • Drive end-to-end business analysis across Veeva Quality Docs and QMS implementation and enhancement projects.
  • Gather, document, and validate business and functional requirements for Veeva Quality Docs and QMS modules.
  • Convert quality processes into user stories, use cases, and functional specifications.
  • Plan and lead workshops and interviews with stakeholders across Quality Assurance, Regulatory Affairs, and Compliance.
  • Align stakeholder groups on project scope and priorities while managing competing interests.
  • Partner with Veeva technical consultants and configuration teams to ensure accurate delivery of requirements.
  • Support the design of document lifecycle workflows and training record structures within Quality Docs.
  • Ensure alignment with GxP, 21 CFR Part 11, and CSV compliance principles.
Education & Experience:
  • 10+ years of experience with Veeva Vault Quality Docs/QMS.
  • 10+ years of Business Analysis experience within the Pharmaceutical/Life Sciences industry.
  • 6+ years of experience with GxP, 21 CFR Part 11, and CSV compliance.
  • Experience with stakeholder management across QA and Regulatory Affairs.
  • Experience in document lifecycle workflow design.
  • Veeva Vault Certification is preferred.
  • Strong written and verbal communication skills.

Numbers & Facts

LocationWarren, NJ

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