Are 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.
About The Role
Location: Ivrea, Italy
Relocation Support: This role is based in Ivrea, Italy. Novartis is unable to offer relocation support: please only apply if accessible.
Major Accountabilities
- Design, execute, interpret, and report analytical studies supporting radioligand therapy development projects.
- Develop, validate, transfer, and maintain analytical methods to agreed quality and timeline standards.
- Coordinate analytical activities and align strategy with cross-functional development project teams.
- Provide scientific expertise and share analytical best practices across teams and functions.
- Support formulation and process development through robust analytical testing and data interpretation.
- Author analytical documentation supporting development, regulatory, and quality requirements.
- Contribute to specification setting and analytical strategy throughout product development stages.
- Support analytical method transfers to manufacturing sites and radiopharmacy partners.
Essential Requirements
- Master’s degree in Chemistry, Pharmaceutical Technology, or a related scientific discipline.
- Minimum two years of industry experience in analytical chemistry, radiochemistry development, or quality control.
- Experience developing and applying analytical methods, including High Performance Liquid Chromatography.
- Knowledge of Good Manufacturing Practice and quality standards supporting drug development.
- Experience authoring
📌 Analytical Expert (Italia)
🏢 Novartis Italia
📍 Italia
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