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Senior Expert Science & Technology - Radiochemistry

Job in 10015, Ivrea, Piemonte, Italy
Listing for: Novartis Pharma Schweiz
Full Time position
Listed on 2026-02-22
Job specializations:
  • Research/Development
    Research Scientist, Medical Science, Data Scientist
  • Healthcare
    Medical Science, Data Scientist
Job Description & How to Apply Below
Location:

Ivrea, Italy #onsite
Role Purpose
The Senior Expert Radiochemistry oversees and executes isotope development projects in close alignment with the Radiochemistry Team Leader and the IDU strategy, serving as a Subject Matter Expert in radiochemistry. The role is prevalently hands‑on in development, execution, and/or optimization of radio chemical separation/purification technologies, target‑related preparation processes, and (radio) analytical methods. In close collaboration with theragnostic and drug product teams, the SME evaluates radionuclide precursor characteristics/specifications and their impact on product development.

Role is complemented by data acquisition, analysis, and interpretation, accompanied by literature research when required. Responsibilities include authoring/revising technical documentation (protocols, reports, SOPs) and supporting change controls, deviations, investigations, and risk assessments as needed. The Senior Expert provides scientific guidance and oversight of internal activities and external partners (CRO/CMO), ensuring high data quality / integrity and timely delivery. The role ensures compliance with applicable quality, safety, and cGMP requirements (where relevant), maintaining equipment readiness and driving continuous improvement.

The role includes supervision and coaching of assigned laboratory associates, ensuring effective resource utilization and active knowledge sharing. The Senior Expert Radiochemistry reports to the Radiochemistry Team Leader.
Major Accountabilities
In alignment with the Team Leader and IDU strategy, contribute to the design and planning of scientific experiments and analysis/interpretation of experimental data; prepare high-quality summaries, reports and other documentation to support internal decision-making and regulatory/registration needs.
Contribute to the development, optimization, and implementation of efficient, robust and safe radionuclide‑related processes and (radio) analytical methodologies, in compliance with relevant quality and regulatory standards (including cGMP where relevant), within agreed timelines and budgets; communicate key advancements and challenges. Plan and execute hands‑on laboratory work safely and efficiently; operate, maintain and troubleshoot a broad range of laboratory and analytical equipment, ensuring proper calibration, qualification, documentation and adherence to internal standards.

Ensure adherence to organizational workflows, procedures, documentation practices and data integrity expectations across laboratory activities.
Provide scientific and technical guidance, actively fostering knowledge exchange within the team and across interfaces; provide technical oversight of external partners (CRO/CMO), including review of protocols, data packages, and deliverables. Author, review, and maintain technical and scientific documentation (protocols, reports, SOPs) and support quality‑system activities (change controls, deviations, investigations, CAPA input, and risk assessments) where needed. Present scientific/technical results internally and contribute to publications, presentations and patents as appropriate, ensuring timely and accurate reporting aligned with internal governance and regulatory requirements.

Supervise, mentor and coach assigned lab and scientific associates (and, where applicable, coordinate external contributors), ensuring efficient resource utilization, clear priority setting and appropriate levels of guidance based on experience and expertise.

Minimum Requirements

Master Degree in Chemistry or related scientific discipline (PhD is a plus)
Strong background in radiochemistry and/or (radio) analytical chemistry
4‑6 years of relevant experience in radiochemistry / radiopharmaceutical or isotope development, including hands‑on work with radioactive materials, radionuclide identification / characterization
Strong knowledge of ALARA principles
Practical experience working in shielded fume hoods, hotcells and/or glove boxes; experience using tele‑manipulators is strongly desired
Demonstrated experience with HPGe spectrometry and related data acquisition and analysis software
Knowledge…
Position Requirements
10+ Years work experience
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