Novartis

QualityControlTechnician

ivrea, piedmont, 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 analysis, cGMP, GxP Compliance, SOPs, Quality Standards, batch analysis, incoming materials analysis, equipment maintenance and calibration, documentation. Perform 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”

What You'll Achieve.

reporting of the QC results; Escalation in case of non-conformances and deviations

Industry & Context.

Problems you'll solve

Escalation in case of non-conformances and deviations; manage these quality incidents; Support deviation investigations; OOS/OOT/OOE investigations

Eligibility Requirements

work in rotating shifts, including night turns

What You'll Do.

Perform 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

makes analysis on batches and incoming materials according to cGMP rules and SOPs

Perform the analysis of batches following specific

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

Perform incoming and outgoing verification activities of raw materials

Execute the calibration

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

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

Prepares applicable documents

and records such as analytical batch records and follows Good Documentation Practices

Support internal and external Audits and Inspections

How You'll Work.

Team & Collaboration

cross-functional coordination; vendor/stakeholder management; Support internal and external Audits and Inspections

Communication Scope

Fluent Italian; good knowledge of English

Process & Methodology

CAPA follow up and implementation, Change Control management

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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