ph3Experteer Overview /h3pIn 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.
Scorra la pagina per visualizzare tutti i requisiti del lavoro e le responsabilità che i candidati selezionati dovranno assumersi.
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.
/ph3Responsibilities /h3ulliManage change controls across sites /liliPlan and execute site trainings /liliIssue and revise Product Quality Reviews (PQR)



/liliParticipate in self-inspections and CAPA management /liliRevise Master Batch Records /liliIssue validation protocols and reports /liliParticipate in risk assessment management /liliCooperate in revising qualification and validation documentation /liliOversee Quality Agreement with customers /liliSupport regulatory activities to maintain manufacturing licenses /liliCollect and monitor site KPIs /li /ulh3Qualifications /h3ulliDegree in Scientific disciplines xrdztoy /lili3–5 years of experience in Quality Assurance within pharmaceutical sector /liliKnowledge of local and international regulatory requirements and GMP standards /liliCompetency in communication and interfaces management /liliFluent English /li /ulh3Benefits /h3ulliPerformance-based annual premio /liliEqual employment opportunities /li /ul /p #J-18808-Ljbffr

📌 Quality Assurance Specialist (Italia)
🏢 Experteer Italy
📍 Italia