REQ-10025711
十一月 11, 2024
Italy

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? https://www.novartis.com/about/strategy/people-and-culture

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Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

International
Innovative Medicines
Italy
Ivrea
Quality
Full time
Regular
No

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

A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
REQ-10025711

QC Analyst

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