Analytical Expert - Science & Technology
Pubblicato il 14-09-2026 - Novartis Italia in Montà
Summary
Are you passionate about advancing groundbreaking radioligand therapies that have the potential to transform patients' lives?
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.
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 Chemistry, Manufacturing and Controls documentation for regulatory submissions.
Strong problem-solving, decision-making, and scientific technical writing skills.
Understanding of the safe handling of chemicals, laboratory materials, and equipment.
Fluent English, both written and spoken is required.
Desirable Skills
Fluency in Italian would be an advantage.
Benefits And Rewards
At Novartis, we are committed to reimagining medicine together—and rewarding the people who make it happen.
Expected annual base salary range for this position: €33,500 to €62,100.
Base 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.
In addition to the base salary, you may be eligible for a performance-based premio, depending on established performance criteria.
The 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.
In addition, we offer flexible and hybrid working arrangements where possible, as well as a minimum of 14 weeks of paid parental leave.
Why Novartis:
Helping people with disease and their families takes more than innovative science.
It takes a community of smart, passionate people like you.
Collaborating, supporting and inspiring each other.
Combining to achieve breakthroughs that change patients' lives.
Ready to create a brighter future together?
Benefits and Rewards:
Read our handbook (PDF 30 MB)
#J-*****-Ljbffr