Qc Analyst

Summary Execution of assigned tasks in the quality control laboratory in accordance with cGxP regulations. Performance of laboratory specific activities such as analyses, maintenance, calibration and qualification of analytical equipment.

About the Role OPERATIONAL Sample storage and management Analytical testing and documentation of incoming materials / drug products / stability / packaging material samples Ensure all activities in compliance with cGxP, incl. data integrity Stability
Testing/Sample storage and management Analytical documentation of stability samples to cGxP standards HSE Comply with all HSE guidelines Detect and report potential accident, risks and propose solutions Responsible for participating in initial training and retraining Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together?

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Job Details Division: International

Business Unit: Innovative Medicines

Location: Italy

Site: Ivrea

Company / Legal Entity: IT58 (FCRS = IT058) AAA Italy Srl.

Functional Area: Quality

Job Type: Full time

Employment Type: Regular

Shift Work: No

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.



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