Job Description Summary
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.
Job Description
Location: Ivrea, Italy
LI-Hybrid
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 support
📌 Analytical Expert (Ivrea)
🏢 Novartis
📍 Ivrea
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