Qa systems specialist
Pubblicato il 15-08-2026 - Jobtailor in OriggioResponsibilities Management of change controls Participation in planning and execution of site trainings Issuance and revision of Product Quality Review (PQR) Participation in planning and execution of self‐inspections together with CAPA management Revision of Master Batch Records Issuance of process validation protocols and reports Participation in risk assessment management Cooperation in the revision of qualification and validation documentation Overview on Quality Agreement with customers Participation in management of regulatory aspects to maintain required manufacturing licenses Collection of site KPIs Requirements Degree in Scientific disciplines 3–5 years of experience in Quality Assurance positions within the pharmaceutical sector Knowledge of the local and international legal/regulatory requirements and GMP standards Competency in communication and interfaces management Fluent English