Computerized System Validation Engineer

Sanrafaelvet

Not specified
Qualification documentation management
Validation protocols and reports
Risk analysis procedures
Sanrafaelvet is seeking a Computerized System Validation Engineer to manage qualification operations within the pharmaceutical industry. The ideal candidate should have at least 2 years of experience in validation, a strong understanding of qualification processes, and proficiency in French for documentation tasks

Job Summary

  • The mission involves following and participating in qualification operations, including the drafting, verification, and management of qualification documentation such as protocols, reports, procedures, and risk analyses.
  • Key activities include drafting qualification documents (QC, IQ, OQ, PQ), monitoring test execution, managing deviations, verifying supplier documents, and participating in qualification committees.
  • The role requires at least 2 years of experience in pharmaceutical industry qualification, with a strong command of French for professional document writing.

Matching Summary

Match Score: 85

Sanrafaelvet is seeking a Computerized System Validation Engineer to manage qualification operations within the pharmaceutical industry. The ideal candidate should have at least 2 years of experience in validation, a strong understanding of qualification processes, and proficiency in French for documentation tasks.

Skills & Requirements

Must-have

  • Qualification documentation management
  • Validation protocols and reports
  • Risk analysis procedures
  • KPI tracking for qualification
  • Coordination with departments and subcontractors

Nice-to-have

  • Continuous process improvement
  • Collaborative team environment
  • Commitment to scientific advancement

Key Requirements

  • Minimum 2 years pharmaceutical qualification experience
  • Engineering, Master, or Bachelor's degree
  • Proficiency in French for document writing

Work Rights

Not specified

Tailored Resume

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