Radiopharmaceutical Production Operator (Shift Work)

Novartis AG

Ivrea

Ibrido

EUR 38.000 - 52.000

Tempo pieno

11 giorni fa
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Vantaggi offerti da questo lavoro

Hybrid working options

Descrizione del lavoro

Novartis AG in Italy is seeking a production operator for radiopharmaceutical manufacturing. The role involves working in shifts, including nights and weekends, to prepare and produce batches in accordance with cGMP and approved SOPs.

You will perform routine maintenance, verification of materials, and collaborate on training and waste management, while reporting any deviations to management. Fluency in Italian and good English are required, with a scientific/technical background guiding

Competenze

  • Production of radiopharmaceuticals according to cGMP and approved SOPs.
  • Perform routine maintenance, cleaning and microbiological verification activities.
  • Report deviations and out-of-specs to Production Manager and Qualified Person.
  • Perform incoming/outgoing verification of raw materials and materials.
  • Collaborate on material stocks and waste management.
  • Collaborate on training of new personnel.
  • Willing to work shifts, including night shifts and weekends.
  • Fluent in Italian; good knowledge of English.

Mansioni

  • Carry out production of radiopharmaceuticals in compliance with cGMP, HSE, and SOPs.
  • Perform routine maintenance and cleaning of pharmaceutical areas and equipment.
  • Support external specialists for maintenance/qualification activities.
  • Report deviations to Production Manager and Qualified Person.
  • Verify incoming and outgoing materials.
  • Assist with stock management and waste handling.
  • Assist in training new personnel.

Conoscenze

Fluent in Italian
Knowledge of English
Shift work readiness
Scientific background

Descrizione del lavoro

Novartis AG in Italy is seeking a production operator for radiopharmaceutical manufacturing. The role involves working in shifts, including nights and weekends, to prepare and produce batches in accordance with cGMP and approved SOPs.

You will perform routine maintenance, verification of materials, and collaborate on training and waste management, while reporting any deviations to management. Fluency in Italian and good English are required, with a scientific/technical background guiding

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