- Ensuring compliance with data protection regulations
- Reviews executed batch records
- Prepares the documentation to be transmitted to the contact givers after batch release
- Gives assessment to the qualified person before batch disposition decision
- Observes all health, safety and environmental protection measures within their area of responsibility
- Complies with quality procedures bases on GxP standards, including active participation in hygiene and good documentary practices
- Providing support for upcoming QA activities
- Bachelor of Science in relevant field (Pharmaceutical industry, Chemistry)
- 1-2 years experience in Pharma / CDMO a plus
- Knowledge of applicable GxP and related guidelines
- Professional in French (both in oral and written communication)
- Professional in English (in written communication)
- Computer skills
