342822BR
Apr 05, 2022
Spain
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
Although this is a shift job (nights from 10 p.m. to 6 a.m. and mornings from 6 a.m. to 2 p.m.), we offer a permanent contract, extensive training and professional stability.
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
Although this is a shift job (nights from 10 p.m. to 6 a.m. and mornings from 6 a.m. to 2 p.m.), we offer a permanent contract, extensive training and professional stability.
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
- Languages: Basic reading/writing/speaking of English (medium or high will be valued)
- Experiences: Previous experience in pharmaceutical or radiopharmaceutical companies is desirable
ONCOLOGY
ADVANCED ACCELERATOR APPLICATIONS
Spain
Zaragoza
AAA Ibérica S.L.U.
Technical Operations
Full Time
Regular
Yes
