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Computer System Validation Engineer

Computer System Validation Engineer

Katalyst HealthCares & Life SciencesSan Juan, PR
Hace 15 días
Descripción del trabajo

Roles & Responsibilities :

  • Full lifecycle validation for all applicable computerized systems, ensuring they are designed, validated, operated and retired in compliance with GxP regulation and computer system validation (CSV) guidance.
  • Compiling and maintaining accurate CSV documentation, ensuring full traceability throughout system lifecycles.
  • Compliance Analysis, Validation Planning, Risk Assessments.
  • Test planning and strategy.
  • creation and execution of test protocols, scripts and reports.
  • Validation Summary Reports, traceability analysis.
  • Defect Logging and Tracking till closure.
  • Develop, approve, and execute validation deliverables for computerized systems, including validation plans, risk assessments, and traceability matrices.
  • Author and update documentation to support ongoing CSV compliance.
  • Prepare or review all levels of validation documents including.
  • Validation (Strategy) Plans, User Requirement Specifications.
  • Definition Documents, including Functional Specifications S / W Design Specifications or Configuration Documents and SOPs.
  • Qualification Documents and Test Specifications (IQ, OQ, PQ).
  • Traceability Matrices, Risk Analysis.
  • Validation Reports, Change Controls / Events / Deviations etc.
  • Assess the impact of changes proposed to computerized systems and the level of change required.
  • Provide validation strategy to the introduction of computerized systems.
  • Collaborate with the key stakeholders (Information Systems, Software assurance, business users and suppliers etc., and management on all related matters on a regular basis.
  • CSV, Validation, Testing, Reports, Test, data validation, GAMP, CFR.
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Validation Engineer • San Juan, PR

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