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

📌 QA Systems Specialist (Varese)
🏢 Grünenthal
📍 Varese