Internship Validation
THE INTERNSHIP
The intern will be part of Qualification & Validation team in the Boehringer Ingelheim production site in Noventa Padovana, where veterinary vaccines are produced.
The intern will be an active part of qualification and validation and periodic review activities.
**We offer a 6 months internship with a possible 6-months extension
**Tasks & what you will be learning:
- Support in qualification/validation activities and periodic review (LeVA methodology)
- Support during the expected test execution activities
- Support for the drafting of GMP quality documentation (validation protocols and reports and local procedures)
- Collaboration with other departments, such as production, laboratory and quality
- Review QA documentation, local and global procedures
- Preparation and participation to department meetings and regulatory inspections Preparation of Excel file and PowerPoint presentation
**Requirements**:
- Master's degree in in scientific disciplines (preferably chemical engineering, industrial chemistry, CTF, Pharmacy)
- Ability to work methodically and carefully according to tight deadlines
- Good Knowledge of the English language (level B2/C1)
- Good Knowledge and autonomy in the use of PC and Office package
- Curious and analytical attitude, propensity for continuous improvement, innovation and teamwork
- Ability to manage priorities and meet deadlines
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