ppThe Equipment Operator ensures the execution of secondary packaging activities for ophthalmic products in compliance with GMP regulations, company procedures, and established quality, safety, and productivity requirements. /ph3Key responsibilities: /h3ulliOperate and run automated secondary packaging lines for ophthalmic products, performing set-up, changeover, and start-up activities. /liliManage the proper feeding of packaging materials and monitor equipment performance, promptly reporting any abnormalities. /liliPerform Line Clearance, Line Checks, and in-process controls to ensure product compliance with quality requirements. /liliVerify correct coding, serialization, aggregation, and readability of variable data, while ensuring proper handling of non-conforming products. /liliOperate in compliance with GMP, Data Integrity, HSE requirements, and company procedures, ensuring full traceability and accurate completion of production documentation. /liliSupport investigations related to process deviations and anomalies, and participate in internal and external audits and inspections. /liliPerform line cleaning activities and collaborate with Quality Assurance, MST, Engineering, and Maintenance to ensure operational continuity. /liliContribute to Continuous Improvement, Operational Excellence, digitalization, qualification, and validation initiatives, helping to reduce waste, line downtime, and deviations. /li /ulh3Essential requirements: /h3ulliTechnical high school diploma or equivalent secondary education qualification, preferably in Mechanical, Electrical, Electronic, or Chemical disciplines; previous experience in the pharmaceutical, medical device, or sterile packaging industry is considered a plus. /liliExperience in manufacturing or industrial packaging operations,



preferably within GMP-regulated environments. /liliKnowledge of Good Manufacturing Practices (GMP) and secondary packaging processes; experience with sterile or ophthalmic product packaging is advantageous. /liliFamiliarity with production IT systems such as MES, SAP, or equivalent platforms, as well as serialization, aggregation, and traceability processes. /liliUnderstanding of vision systems, checkweighers, laser/inkjet printers, Track Trace solutions, and quality inspection cameras. /liliStrong attention to detail, accuracy in documentation, and a quality-and compliance-focused mindset with a strong commitment to safety and procedural adherence. /liliEffective teamwork, operational problem-solving skills, flexibility, continuous improvement mindset, and the ability to identify and elevate quality risks and process deviations. /liliAvailability to work in shifts and participate in ongoing training; contributes to achieving key performance indicators including production plan adherence, "Right First Time", waste and deviation reduction, GMP compliance, audit readiness, line efficiency (OEE), and documentation accuracy. /li /ulh3Commitment to Diversity Inclusion: /h3pWe are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. /ph3Why Novartis? /h3pOur purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. With our people, it is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! /ph3Accessibility and accommodation: /h3pNovartis is committed to working with and providing reasonable accommodation to all individuals. /p /p #J-18808-Ljbffr

📌 Equipment Operator (Torre Annunziata)
🏢 Biopharma Careers
📍 Torre Annunziata