PpLocation: Ivrea, Italy /ph3Role Purpose /h3pAct as Isotope Project Lead (IPL) by providing specialist knowledge and expertise as a Subject Matter Expert (SME) of radioisotope production and purification, focusing on assessing, developing, and optimizing new technologies that support radioligand therapy (RLT) products Life Cycle Management (LCM). Develop, optimize, and transfer radioisotope production and purification/separation processes. /ppThis work is done in close collaboration with relevant development centers and Contract Manufacturing Organizations (CMOs). /ph3Major Accountabilities /h3ulliManage inter‑functional project plan and budget using the Project Planning tool or system. /liliIdentify issues and potential bottlenecks within projects and propose options. /liliContribute to Radioisotope TRD‑related activities. /liliEnsure constant technological survey of the radioisotopes production field. /liliApply scientific/technical expertise to identify new programs of interest, and support their development from early evaluation through late phase supply. /liliParticipate in development programs and activities around isotopes, adhering to the global Isotope strategy and objectives within agreed timelines and budgets, reporting key advancements and challenges. /liliIdentify strategic external partners for research collaboration agreements to develop new production technologies or access to innovative isotopes. /liliImplement strategic policies when selecting methods, techniques, and evaluation criteria for achieving results. /liliEstablish and assure adherence to budgets, schedules, work plans, and performance requirements. /liliRepresent the area as a core member in Global Project Teams to define global scientific strategy for development up to submission and approval in major markets of assigned products. /liliReport technical complaints, adverse events, or special case scenarios related to Novartis products within 24 hours of receipt. /li /ulh3Minimum Requirements /h3ulliBSc. in Chemical Engineering, Pharmaceutical Technology, or an equivalent scientific degree. /liliDesirable: MSc., PhD, or equivalent experience. /liliDesirable degree in Radiochemistry and strong scientific knowledge in nuclear medicine. /liliSuccessfully demonstrated at least 5 years of directly related experience in a scientific area or Ph.D. or equivalent. /liliProven project leadership in all project phases. /liliProven process understanding (Pharma, GMP, Validation and Regulatory aspects). /liliSound experience with data handling and applied statistics. /liliStrong understanding of risk assessment and risk management fundamentals/tools. /liliQuality‑oriented with attention to detail. /liliExcellent verbal and written communication skills. /liliExcellent problem‑solving and decision‑making skills. /liliDefining and implementing productivity improvement measures. /liliItalian language proficiency required as a site language. /li /ulh3Commitment to Diversity and Inclusion /h3pNovartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. /p /p #J-18808-Ljbffr