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CSV Engineer

Raritan, NJ
Permanent
Roles & Responsibilities
  • Lead end-to-end CSV activities (inventory assessment remediation disposition)
  • Support business separation for large GxP systems
  • Define & implement risk-based validation strategies
  • Review & approve test plans, UAT scripts, validation documents
  • Ensure compliance with regulatory & quality standards
  • Provide guidance, escalation & leadership to validation teams
  • Collaborate with global & remote teams
Education & Experience :
  • 7 10 years in CSV / Validation roles
  • Experience in Pharma / Biotech / Medical Devices industry
  • Proven experience in regulated environments (FDA/GxP)
  • Strong expertise in CSV (Computer System Validation) in GxP environments
  • Experience in ERP, Data Migration & Cloud Migration (Divestiture/Separation)
  • Hands-on in Acquisitions / Divestitures / Business Separation projects
  • Deep understanding of FDA regulations & GxP standards
  • Experience with Risk-based validation approach
  • Strong knowledge of validation documentation (VP, URS, IQ/OQ/PQ, TSR, SOPs)
  • Experience in UAT, Traceability Matrix & QA methodologies
  • Ability to lead teams & manage multiple projects

Job Type: Permanent

Job ID: 253248984