Lieu Grand Est
Type d'expertise Life Science
Type of Contract CDI

As the Qualification & Validation Engineer, you will be responsible for qualifying laboratory, production, and/or utility equipment. You will be directly integrated into a project team and will ensure compliance with GxP requirements and company regulations.

Your role will include:

  • Planning validation and qualification strategies in accordance with all relevant parties (production/QA/maintenance/C&M).
  • Liaising with equipment suppliers to conduct functional analyses.
  • Planning and coordinating commissioning activities at the supplier’s site (FAT) and in the production environment (SAT).
  • Drafting protocols and participating in IQ/OQ/PQ execution.
  • Developing associated reports.
  • Monitoring the progress of qualification steps and associated reports.
  • Providing proactive analysis and suggestions in all situations.
  • Mastering the entire process.

A graduate of an engineering school or equivalent with a BAC+5 degree, you should have at least one experience in a similar position. You possess a technical background and are interested in project-based work. This role demands a high level of precision due to the requirements of the pharmaceutical field and a capacity to comprehend processes to ensure compliance.


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