Radioligand Therapy Analytics Specialist

Novartis Italia

Ivrea

Ibrido

EUR 34.000 - 62.000

Tempo pieno

2 giorni fa

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Generatore di candidature

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Vantaggi offerti da questo lavoro

Insurance plans

Retirement plans

Wellness resources

Global recognition programs

Hybrid working

Parental leave (14 weeks)

Descrizione del lavoro

Novartis Italia in Ivrea, Italy, is seeking an Analytical Expert to lead analytical strategies for radioligand therapy development. You will design, validate and transfer analytical methods, interpret data, and support development to regulatory milestones.

Ideal candidates hold a Master's in chemistry or related field, have 2+ years in analytical chemistry or radiochemistry, and are fluent in English. The role offers hybrid working arrangements and relocation not covered.

Competenze

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.
Fluency in Italian would be an advantage.

Mansioni

Design, execute, and report analytical studies for radioligand therapy projects.
Develop, validate, transfer, and maintain analytical methods to quality and timeline standards.
Coordinate analytical activities and align strategy with cross-functional teams.
Provide scientific expertise and share analytical best practices across teams.
Support formulation and process development through analytical testing and data interpretation.
Author analytical documentation to support development, regulatory, and quality requirements.
Contribute to specification setting and analytical strategy across product development stages.
Support analytical method transfers to manufacturing sites and radiopharmacy partners.