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Computer System Assurance (CSA) Consultant
Computer System Assurance (CSA) ConsultantKatalyst HealthCares & Life Sciences • Remote, NJ
Computer System Assurance (CSA) Consultant

Computer System Assurance (CSA) Consultant

Katalyst HealthCares & Life Sciences • Remote, NJ
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Summary :

We are seeking an experienced Computer System Assurance (CSA) Consultant to support GxP compliance activities across Clinical, and Regulatory Affairs systems. This role will work closely with Quality, IT, and business stakeholders to ensure systems are implemented, maintained, and operated in compliance with applicable regulations and internal procedures.

Roles & Responsibilities

  • Provide CSA / CSV subject matter expertise across PV, Clinical, and Regulatory Affairs platforms
  • Support system implementations, enhancements, integrations, upgrades, and data migrations from a compliance perspective
  • Develop and review validation deliverables including Validation Plans, Risk Assessments, Traceability Matrices, and Validation Summary Reports
  • Review and approve lifecycle documentation (URS, specifications, test plans, test summaries) in alignment with ALCOA+ and Good Documentation Practices
  • Oversee validation readiness and ensure prerequisites are met prior to formal testing
  • Support change control, configuration management, and release activities
  • Partner with Quality, System Owners, and Business Process Owners to ensure ongoing compliance
  • Provide guidance on CSA-based, risk-driven validation approaches

Education & Experience :

  • – years of hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains
  • Hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains
  • Strong understanding of CSA principles, CSV, and SDLC processes
  • Experience authoring and / or reviewing validation documentation
  • Working knowledge of GxP regulations (, FDA, EMA, ICH) and data integrity expectations
  • Ability to work independently in a fast-paced, matrixed environment
  • Strong communication skills and comfort interacting with Quality and business stakeholders
  • Experience with enterprise platforms supporting PV, Clinical, or Regulatory operations
  • Prior role as a Validation SME, CSA Lead, or Compliance Consultan
  • Familiarity with electronic quality systems, change management tools, or application lifecycle management platforms
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