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