06 ago
|
Productlife Group
|
Italia
06 ago
Productlife Group
Italia
Specific activities and responsibilities:
- Plan, coordinate, and execute Computerized System and SW applications Validation (CSV) activities for client projects in compliance with GAMP 5, GMP, EU GMP Annex 11, and 21 CFR Part 11 requirements.
- Prepare, review, and manage validation documentation, including Validation Plans, Risk Assessments, URS, IQ/OQ/PQ protocols, and Validation Reports.
- Support clients in ensuring Data Integrity compliance in accordance
📌 Validation Specialist (Italia)
🏢 Productlife Group
📍 Italia