ppSalary Range: €33,500.00 - €62,100.00 /ph3Job Description Summary /h3pAre you passionate about advancing groundbreaking radioligand therapies that have the potential to transform patients' lives? As an Analytical Expert, you will play a pivotal role in developing and delivering innovative analytical strategies that support the development of radioligand drug substances and drug products. Working alongside talented cross-functional teams, you will apply scientific expertise, drive analytical excellence, and contribute to bringing high-quality therapies from development to patients worldwide. /ph3Job Location and Format /h3pLocation: Ivrea, Italy /ppHybrid: #LI-Hybrid /ppRelocation support: This role is based in Ivrea, Italy. Novartis is unable to offer relocation support: please only apply if accessible. /ph3Major Accountabilities /h3ulliDesign, execute, interpret, and report analytical studies supporting radioligand therapy development projects. /liliDevelop, validate, transfer, and maintain analytical methods to agreed quality and timeline standards. /liliCoordinate analytical activities and align strategy with cross-functional development project teams. /liliProvide scientific expertise and share analytical best practices across teams and functions. /liliSupport formulation and process development through robust analytical testing and data interpretation. /liliAuthor analytical documentation supporting development, regulatory, and quality requirements. /liliContribute to specification setting and analytical strategy throughout product development stages. /liliSupport analytical method transfers to manufacturing sites and radiopharmacy partners. /li /ulh3Essential Requirements /h3ulliMaster's degree in Chemistry, Pharmaceutical Technology, or a related scientific discipline. /liliMinimum two years of industry experience in analytical chemistry,



radiochemistry development, or quality control. /liliExperience developing and applying analytical methods, including High Performance Liquid Chromatography. /liliKnowledge of Good Manufacturing Practice and quality standards supporting drug development. /liliExperience authoring Chemistry, Manufacturing and Controls documentation for regulatory submissions. /liliStrong problem-solving, decision-making, and scientific technical writing skills. /liliUnderstanding of the safe handling of chemicals, laboratory materials, and equipment. /liliFluent English, both written and spoken is required. /li /ulh3Desirable Skills /h3ulliMaterials Science, Process Simulation, Technical Writing, Waterfall Model. /liliFluency in Italian would be an advantage. /li /ulh3Benefits and Rewards /h3ulliExpected annual base salary range for this position: €33,500 to €62,100. /liliBase salary is determined using gender-neutral criteria such as relevant skills, competencies, and experience, in accordance with Novartis compensation policies, and is reviewed regularly after joining Novartis. /liliIn addition to the base salary, you may be eligible for a performance-based premio, depending on established performance criteria. /liliThe rewards of being part of our team extend far beyond base pay and incentives. /liliWe also offer a variety of competitive benefits designed to support your personal and professional well-being, including insurance plans, retirement plans, wellness resources, and global recognition programs. /liliIn addition, we offer flexible and hybrid working arrangements where possible, as well as a minimum of 14 weeks of paid parental leave. /li /ulh3Ready to help shape the future of radioligand therapies? /h3pJoin Novartis and apply your scientific expertise to deliver innovative medicines that can transform patients' lives. /p /p #J-18808-Ljbffr

📌 Analytical Expert - Science & Technology (Ivrea)
🏢 IT58 (FCRS = IT058) Advanced Accelerator Applications Italy
📍 Ivrea