Summary
About the Role
Major accountabilities:
- Perform the analysis of batches following specific training;
- Promptly report to the Quality Control Supervisor and the Qualified Person any deviation and/or out of specification detected during the analysis activities.
- Collaborate with the Quality Control Head/supervisor for the CAPA implementation in the quality control department.
- Control processes, equipment and area.
- Perform routine maintenance and cleaning, periodic microbiological verification of pharmaceutical areas quality control equipment and support external specialized personnel in carrying out extraordinary maintenance/qualification activities.
- Perform incoming and outgoing verification activities of raw materials and materials.
- Collaborate with the Quality Control Head to the management of material stocks and waste materials.
- Collaborate with the Quality Control Head to the training of new personnel.
- Execute the calibration, verification, qualification and validation activities of the Quality Control processes and equipment.
Essential requirements:
- Degree in CTF, Pharmacy, Chemistry.
- Previous experience in a similar role within a laboratory or a GMP environment.
- Available to work in shifts, including night shifts.
- Fluent in Italian. Good knowledge of English.
This is a site-based role in Ivrea and it requires to work in shifts, including night shifts and weekends.
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