REQ-10025711
Nov 11, 2024
Italy

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

Role Requirements

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

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

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
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REQ-10025711

QC Analyst

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