Description
Responsibilities- Writing and performing Deviation / CAPA investigations into product issues
- Liaising with local QA and Manufacturing staff to ascertain information in order to understand aseptic production processes and products
- Working to tight deadlines
Experience
- 1-2 years experience working in Quality Assurance within the Pharmaceutical industry handling deviations and ultimately CAPAs
- Understanding of aseptic production processes, ideally injectables
- A background in Microbiology would also be advantageous
- Qualification in Chemistry, Pharmacy or Biology
- Fluent Italian and English in written and oral communication