Sep 23, 2022

Job Description

Job Purpose
Carry out the production of radiopharmaceuticals according to cGMP rules and approved SOPs.

Major Accountabilities
• Working in shifts, perform the necessary activities for the preparation and production of batches
• Comply with the relevant procedures and indications as well as maintain the operational excellence of the Site
• 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
• Collaborate with the Production Manager and the Qualified Person to the CAPA implementation for the production areas and processes

We offer a permanent contract, extensive training and professional stability. This is the opportunity to work in a multinational company (growing and expanding), doing a task that impacts directly on cancer patients’ lives.

Keep in mind this a shift job, and the site is located in La Almunia de Doña Godina.

Diversity & Inclusion / EEO

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

Minimum Requirements

- Education: Scientific background
- Languages: Basic reading/writing/speaking of English (medium or high will be valued)
- Experiences: Previous experience in pharmaceutical or radiopharmaceutical companies is desirable
Technical Operations
Full Time
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Production Technician

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