04 set - Ivrea
Biopharma Careers
ppAre 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. /ppLocation: Ivrea, Italy#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 /h3ulliFluency 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. We 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 /ul /p #J-18808-Ljbffr
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