Computerized System Validation Engineer

Sanofi

Not specified
Qualification documentation management
Qualification operations tracking
Risk analysis documentation
Sanofi is seeking a Computerized System Validation Engineer to participate in qualification operations and documentation management within the pharmaceutical industry. The ideal candidate should have at least two years of experience in qualification and be proficient in French

Job Summary

  • The mission involves following and participating in qualification operations, including writing, verifying, and managing qualification documentation such as protocols, reports, procedures, and risk analyses.
  • Key activities include drafting qualification documents (QC, QI, QO, QP, computerized systems), monitoring test execution, managing deviations, and verifying supplier documents.
  • The role requires contributing to qualification committees, preparing presentations, tracking progress, and managing qualification documentation lifecycle.

Matching Summary

Match Score: 85

Sanofi is seeking a Computerized System Validation Engineer to participate in qualification operations and documentation management within the pharmaceutical industry. The ideal candidate should have at least two years of experience in qualification and be proficient in French.

Skills & Requirements

Must-have

  • Qualification documentation management
  • Qualification operations tracking
  • Risk analysis documentation
  • Coordination with departments and subcontractors
  • KPI calculation and tracking

Nice-to-have

  • Desire to make miracles happen
  • Commitment to diversity and inclusion

Key Requirements

  • Minimum 2 years pharmaceutical qualification experience
  • Engineering, Master's, License, or Pharmacy degree
  • Proficiency in French for professional documentation

Work Rights

Not specified

Tailored Resume

Cover Letter