Overview In Grünenthal’s Manufacturing & Global Operations, you help safeguard product quality across the value chain by leading change controls, PQR issuance, CAPA-driven improvements, and master data validation. You collaborate with cross-functional teams to ensure regulatory compliance and licensing obligations are met while driving continuous quality improvements. This role offers hands-on QA responsibilities with meaningful impact on patient safety and product excellence.

Retribuzione / Benefits

performance-based annual premio equal employment opportunities

Responsabilità

Manage change controls across sites Plan and execute site trainings Issue and revise Product Quality Reviews (PQR)



Participate in self-inspections and CAPA management Revise Master Batch Records Issue validation protocols and reports Participate in risk assessment management Cooperate in revising qualification and validation documentation Oversee Quality Agreement with customers Support regulatory activities to maintain manufacturing licenses Collect and monitor site KPIs

Requisiti fondamentali

Degree in Scientific disciplines 3–5 years of experience in Quality Assurance within pharmaceutical sector Knowledge of local and international regulatory requirements and GMP standards Competency in communication and interfaces management Fluent English communication stakeholder management team collaboration GMP knowledge regulatory compliance CAPA

📌 Senior QA Systems Specialist (Origgio)
🏢 Grünenthal
📍 Origgio