Quality Assurance Internship in Scoppito, Italy. Responsibilities include supporting the GMP production documentation review (Batch Records, deviations, complaints, AQL), data collection for Product Quality Review (PQR) revisions, learning production processes and flows in a pharmaceutical facility, ensuring proper archival of quality, analytical and production documentation, and assisting with investigations and special lot management. Requires a scientific degree (pharmacy, chemistry, biology, etc.), good English (B2+), and own transportation. The internship lasts 6 months and is conducted on-site with expense reimbursement and access to the company canteen.
Details
- Work type
- Onsite
- Remote eligible
- No
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