Associate Scientist Technical Development

3 giorni fa

Ivrea, Piemonte, Italia Novartis A tempo pieno
Summary

Plan, perform and report scientific experiments with SME (subject matter expert) to support the innovation projects and/or advance the innovation technical platform of radiopharmaceutical parenteral dosage forms. Contribute to maintenance of laboratory instruments/infrastructure.

About the Role

Key responsibilities

  • Plan and execute characterization studies, analytical tests, and method development with the innovation project leader (e.g., HPLC purity, UV content, identity, pH, osmolality, visible particles).
  • Perform literature searches, support innovation, contribute to RLT IP and platforms, and share learnings across local/global teams.
  • Provide raw data documentation, contribute to result interpretation, and ensure all documentation is correct, structured, complete, and compliant with SOPs, HSE, and AdAcAp/Novartis guidelines.
  • Maintain clean and tidy work areas, including proper waste management, and keep accurate records of chemicals, intermediates, excipients, and solvents.
  • Ensure correct and timely completion of logbooks and eLN experiments according to local procedures.
  • Strictly follow HSE rules, laboratory workflows, and procedures related to shipments and materials management.
  • Keep all required training up to date with no overdue assignments without acceptable cause.
  • Act as an ambassador for the Novartis mindset, fostering a collaborative, curious, and courageous working style and applying continuous improvement principles.

Essential requirements:

  • Master's degree in a scientific field and 1–3 years of relevant pharmaceutical/biotech industry experience
  • Good English skills (oral and written) and fluent in the local site language
  • Awareness of safe handling of chemicals, hazardous materials, and laboratory/technical equipment
  • Adequate scientific or technical knowledge in a specific area (e.g., synthetic, analytical, pharmaceutical)
  • Good knowledge of pharmaceutical quality control and production processes
  • Adequate knowledge in related scientific/technical collaboration areas
  • Good knowledge of laboratory and/or technical tools, including relevant software and computer tools
  • Basic presentation and scientific/technical writing skills

Why Novartis? Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Learn more here:

You will receive: You can find everything you need to know about our benefits and rewards in the Novartis Life

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here:

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 to learn about all the ways we'll help you thrive personally and professionally:

Division

Development

Business Unit

Development

Location

Italy

Site

Ivrea

Company / Legal Entity

IT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl

Functional Area

Research & Development

Job Type

Full time

Employment Type

Temporary (Fixed Term)

Shift Work

No

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Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

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