Computer Systems Validation Specialist

Madison-Davis
  • Bridgewater, NJ
  • Instant Apply
3 days ago

Job Description


A biopharmaceutical organization is seeking an experienced Computer Systems Validation Specialist to support business-application implementation projects and ongoing system changes.

This position will provide CSV strategy, validation documentation leadership, and project-level coordination to ensure computerized systems are implemented and maintained in accordance with regulatory and quality requirements.

The ideal candidate will bring hands-on validation experience, strong technical writing skills, independent judgment, and a practical risk-based approach to computerized-system compliance.

RESPONSIBILITIES
  • Develop risk-based CSV strategies for new implementations and existing system changes.
  • Author Validation Plans, Validation Summary Reports, and other key validation deliverables.
  • Collaborate on functional requirements, specifications, and IQ/OQ/PQ documentation.
  • Coordinate CSV deliverables across concurrent implementation projects.
  • Provide guidance during test execution and review executed protocols.
  • Maintain and route validation documentation through Veeva approval workflows.
  • Ensure computerized systems remain compliant with applicable GxP regulations and internal standards.
  • Partner with IT, QA, and business system owners to support successful system validation.

Role Requirements
  • Approximately 5 to 10 years of relevant Computer Systems Validation experience.
  • Hands-on experience supporting GxP computerized-system validation.
  • Strong authorship experience with Validation Plans and Summary Reports.
  • Ability to develop and execute risk-based CSV strategies.
  • Experience validating software implementations and system enhancements.
  • Experience with Veeva systems and validation processes.
  • Understanding of GAMP 5, Category 5 systems, 21 CFR Part 11, Annex 11, and relevant GxP requirements.
  • Familiarity with Computer Software Assurance, data integrity, and IQ/OQ/PQ processes.
  • Strong technical writing, project coordination, and stakeholder communication skills.
  • Bachelor's degree in Computer Science, Engineering, Life Sciences, or a related field.

PREFERRED EXPERIENCE
  • Experience with AI application validation or qualification.
  • Experience assessing GxP implications of AI-related use cases.
  • Exposure to additional Veeva business applications and training-related systems.

Numbers & Facts

LocationBridgewater, NJ

Skills

  • Artificial Intelligence (AI)unmatched
  • Biologyunmatched
  • Business Solutionsunmatched
  • Code of Federal Regulationsunmatched
  • Communication Skillsunmatched
  • Computer Scienceunmatched
  • Computer Softwareunmatched
  • Computer Systemsunmatched
  • Data Qualityunmatched
  • Documentationunmatched
  • GxPunmatched
  • Leadershipunmatched
  • People Managementunmatched
  • Process Validationunmatched
  • Project/Program Coordinationunmatched
  • Quality Assuranceunmatched
  • Regulationsunmatched
  • Riskunmatched
  • Software Administrationunmatched
  • Software Validationunmatched
  • System Validationunmatched
  • Technical Writingunmatched
  • Validation Documentationunmatched
  • Validation Planunmatched
  • Writing Skillsunmatched

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