Novartis

QualityControlTechnician

€33–45k ~AI est. Ivrea, Italy FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Quality Control Technician at Novartis. Skills: Quality Control, GxP Compliance, Laboratory Instrumentation. Perform analysis of batches. Perform routine maintenance”

Industry & Context.

Eligibility Requirements

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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