
Analyst Technician
- Centre-Val de Loire
- CDI
- Temps-plein
- Perform analyses and controls on raw materials, in-process products, and finished products as part of routine and/or stability testing, in accordance with various monographs, while respecting quality and safety procedures, optimizing work and equipment to meet required deadlines.
- Interpret analysis results and write reports (analytical notebooks, certificates of analysis).
- Complete control documentation (log book, equipment tracking notebooks, reagent tracking sheets).
- Suggest changes and improvements in accordance with GMP and ISO 13485 standards, registration files, and Pharmacopoeia requirements and other applicable standards.
- Conduct a preliminary investigation with the help of management in case of anomalies.
- Verify analytical results in compliance with internal rules.
- Participate in the GMP evolution of the laboratory, its logistical organization, and the improvement of equipment usage procedures.
- Contribute to maintaining good working conditions both in relational and safety aspects within Quality Control.
- Scientific studies.
- Professional experience in Quality Control.
- Good theoretical knowledge in chemistry.
- Knowledge of GMP applied to the Quality Control environment.
- Knowledge of control techniques.
- Rigorous and synthetic mindset.
- Practical, reliable, autonomous by nature.
- Good communication.
- Ability to take initiatives and reflect on situations.
- Proficiency in office software Word and Excel.
- Ability to use laboratory equipment control and data acquisition software.