**THE INTERNSHIP
**We offer a 6 months internship with a possible 6-months extension
**Tasks & what you will be learning:
- Support to the Master Batch Record Robustness Project;
- Support for the drafting of GMP quality documentation;
- Learning of the management system of the Quality
- Learning procedures applied within the site
- Review Quality documentation, local and global procedures; Preparation and participation to the regulatory inspections **Requirements**: - Master’s degree in Chemistry, CTF, Pharmaceutical or Biology
- Good organizational skills and ability to work in team/ individually
- Ability to work methodically and carefully according to tight deadlines
- Knowledge of European Pharmacopeia and Good Manufacturing practice (GMP)
- Good Knowledge of the English language (level B2/C1)
- Good Knowledge of Microsoft Office Package
- Curious and attitude, propensity for continuous improvement, innovation and teamwork
- Ability to manage priorities and meet deadlines

📌 Internship Batch Disposition (Noventana)
🏢 BI AH IT
📍 Noventana