Novartis
QualityControlTechnician
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Quality Control Technician at Novartis. Skills: Quality Control, GxP Compliance, Laboratory Instrumentation. Perform analysis of batches. Perform routine maintenance”
Industry & Context.
Rotating shifts, Night turns
What They're Looking For.
Must Have
Chemical or biological degree
Nice to Have
Previous experience in radiopharmaceutical companies, Fluent Italian, Good knowledge of English
What You'll Do.
Perform analysis of batches
Perform routine maintenance
Perform periodic microbiological verification
Support external specialized personnel
Perform incoming verification
Perform outgoing verification
Execute calibration activities
Execute verification activities
Execute qualification activities
Execute validation activities
Oversight on manufacturing
QC sampling activities
Finished Product testing
Environmental Monitoring testing
Reporting of QC results
Escalation in case of non-conformances
Escalation in case of deviations
Manage quality incidents
Support deviation investigations
Support OOS investigations
Support OOT investigations
Support OOE investigations
Change Control management
Participation in qualification activities
Participation in validation activities
Prepares applicable documents
Follows Good Documentation Practices
Support internal Audits
Support external Audits
Full Job Description
**Job Description Summary** The QC Technician performs Quality control analysis on finished Product as well as in incoming materials according to cGMP r and SOPs, performs routine GxP Compliance/ Operational activities according to Novartis Quality Standards and makes analysis on batches and incoming materials according to cGMP rules and SOPs. **Job Description** ** _In this role you will be required to work in rotating shifts, including night turns._** **Major accountabilities:** * Perform the analysis of batches following specific training; * 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; * Execute the calibration, verification, qualification and validation activities of the Quality Control processes and equipment * Responsible for the oversight on manufacturing for QC sampling activities. * Raw Material and Finished Product testing, Environmental Monitoring and Sterility QC testing, and reporting of the QC results. Escalation in case of non-conformances and deviations and manage these quality incidents as per AAA procedures. * Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow up and implementation, and Change Control management, including procedure and form revisions. * Participation in assigned qualification/validation activities, as necessary. * Prepares applicable documents, forms, and records such as analytical batch records and follows Good Documentation Practices. * Support internal and external Audits and Inspections, as required. **Minimum Requirements:** * Education: Chemical or biological degree is desirable. * Previous experience in radiopharmaceutical companies is desirable * Fluent Italian, good knowledge of English. **Why Novartis?** Our purpose is
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