Role Purpose Act as Isotope Project Lead (IPL) providing specialist knowledge as Subject Matter Expert (SME) of radioisotope production and purification, focusing on assessing, developing and optimizing new technologies that support RLT products Life Cycle Management (LCM). Location: Ivrea, Italy (onsite) Responsibilities Manage inter functional project plan and budget using the Project Planning tool or system Identify issues and potential bottlenecks within projects and propose options Contribute to the Radioisotope TRD-related activities. Ensure constant technological survey on the field of radioisotopes production. Apply scientific/technical expertise to identify new programs of interest for the company and support their development from early evaluation up to late phase supply. Participate in development programs and activities around isotopes in adherence with global Isotope strategy and objectives within agreed timelines and budget, timely report key advancements and challenges. Identify strategic external partners for the activation of research collaboration agreement to develop new production technologies/access to innovative isotopes. Implement strategic policies when selecting methods, techniques, and evaluation criteria for obtaining results. Establish and assure adherence to budgets, schedules, work plans, and performance requirements. Represent area as core member in the Global Project Teams for defining global scientific strategy for development up to submission and approval in major markets of assigned product(s). Report technical complaints/adverse events/special case scenarios related to Novartis products within 24 hours of receipt Minimum Requirements BSc. in Chemical Engineering, Pharmaceutical Technology, or equivalent scientific degree. Desirable MSc., PhD or equivalent experience. Desirable degree in Radiochemistry and strong scientific knowledge in nuclear medicine. Successfully demonstrated several years (minimum of 5 years) of directly related experience in a scientific area or Ph.D. or equivalent. Proven Project Leadership in all project phases. Proven process understanding (Pharma, GMP, Validation and Regulatory aspects). Sound experience of data handling and applied statistics is a must. Strong understanding of risk assessment and risk management fundamentals/tools. Quality-oriented with attention to detail. Excellent verbal and written communication skills. Excellent problem solving and decision-making skills. Defining and implementing productivity improvement measures. Italian language needed as a site language. Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. #J-18808-Ljbffr