pIn this role you drive the validation and qualification of automatic inspection systems used for sterile injectable manufacturing, ensuring compliance with GMP, FDA, and EMA standards. You will own technical documentation and participate in new product introduction projects, collaborating with cross-functional teams to optimize inspection recipes and system setups. Your work supports regulatory submissions and continuous process improvements, contributing to reliable, compliant manufacturing. This position offers a hands‑on opportunity to shape automation strategies within a large, values‑driven organization.



/pulliIssue validation-related documents for automatic inspection systems and define setup/qualification strategies /liliDevelop and optimize inspection recipes for new and existing products /liliProvide technical expertise and troubleshooting to support operational activities /liliParticipate in project teams to discuss technical aspects of new product introduction for regulatory submission /liliDegree in Engineering or similar scientific degrees or consolidated experience /liliPrevious pharma experience or validation experience is helpful /liliExperience with automated inspection systems (Körber, Optrel, Innoscan, SEA Vision or similar) is helpful /liliProficient English (written and spoken) /liliIT knowledge: Trackwise, Minitab and Microsoft Office tools /liliExcellent interpersonal skills, proactivity, team-oriented /li /ul #J-18808-Ljbffr

📌 Vision systems project engineer (Monza)
🏢 Experteer Italy
📍 Monza