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Salary
$29k – $54k per year
Location
Hybrid (Ivrea, Italy)
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 20, 2026. First seen by Alion on Sep 22, 2026. Novartis scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Novartis is a Swiss pharmaceutical company created in 1996 by the merger of Ciba-Geigy and Sandoz, two Basel chemical and drug houses with roots in the nineteenth century. It has spent the past decade narrowing itself into a pure innovative medicines business, spinning off its generics arm as Sandoz in 2023 and its eye care business as Alcon in 2019, and now concentrates on cardiovascular, immunology, neuroscience and oncology, including radioligand therapies and gene therapy. Headquartered in Basel and listed in Zurich and New York, it is among the largest research spenders in the industry.

Salary Range:

26.000,00 € - 48.400,00 €

Job Description Summary

Carry out the production of radiopharmaceuticals according to cGMP, HSE rules and approved SOPs.

Job Description

Major accountabilities:

  • Working in shifts, perform the necessary activities for the preparation and production of batches.
  • Perform routine maintenance and cleaning, periodic microbiological verification of pharmaceutical areas and equipment and support external specialized personnel in carrying out extraordinary maintenance/qualification activities.
  • Promptly report to the Production Manager and the Qualified Person any deviation and/ or out of specification detected during the production process.
  • Perform incoming and outgoing verification activities of raw materials and materials.
  • Collaborate with the Production Manager to the management of material stocks and waste materials.
  • Collaborate with the Production Manager to the training of new personnel.

Essential Requirements:

  • Scientific/technical background.
  • Willing to work in shifts, including night shifts and weekends.
  • Fluent in Italian. Good knowledge of English.

Benefits & Rewards

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.

In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Read our brochure to learn more about our global total rewards offering:

https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

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.

Skills Desired

Forklift Operations, GMP Compliance, Health, Safety, and Environment (HSE) Policy, Inventory Management, Machine Operations, Manufacturing, Operations Management, Process Improvements, Production Management, Quality Control (QC), Regulatory Documents
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