Validation engineer aseptic manufacturing
EngiFlex
- Rosia, Siena
- Tempo indeterminato
- Full time
- Commissioning and qualification of new and existing equipment
- Assuring appropriate risk management in the validation strategy
- Writing URS of pharma equipment
- Performing testing and validation activities (FAT and SAT)
- Ensuring that adequate documentation is available for operations and QA
- You will be working in cross-functional teams in a project or operational environment
- Experience in the pharmaceutical sector as validation or C&Q engineer
- Experience in commissioning and qualification of equipment or processes such as formulation, filling, cleaning, sterilization
- Candidate must speak fluent English. Italian is an asset. Dutch is not required.
- The location of the project is NORTHERN ITALY with a good airplane connection to Brussels