Within a competitive and multi-skilled group at the service of the pharmaceutical industry, your duties will be:

  • Optimizing the operating procedures
  • Drafting the new documents, and standardizing the existing ones
  • Monitoring the implementation of improvements
  • Setting up and monitoring a dashboard of non-quality and cost of non-quality

1 year full-time fixed-term contract

Job based near Orléans (45)

If you’re interested, please apply through our contact form.