QC Specialist I

2 days ago

Singapore Novartis Singapore Full time

Join to apply for the QC Specialist I - Analytical role at Novartis Singapore .

This role is responsible for establishing and ensuring testing of drug substance release and stability testing, including testing of intermediates in process control samples. Laboratory operations must comply with written testing SOPs and local/international regulations.

About The Role

Key Responsibilities:

  • Sample storage and management.
  • Analytical testing and documentation of API / drug substance / drug product / finished product / complaints / stability / packaging material samples.
  • Ensure all activities comply with cGxP, including data integrity.
  • Stability testing and sample management when not centralized, with documentation to cGxP standards.
  • Detect and report potential accidents and risks, proposing solutions.

Essential Requirements

  • Experience working in a pharmaceutical laboratory environment, including quality assurance, production, and aseptic techniques.
  • Administrative skills and GMP/HSE compliance for efficient documentation and task execution.
  • Skills in Breakthrough Analysis, Resilience, Operational Excellence, Continuous Learning, and Digital & Tech Savvy.
  • Knowledge of laboratory equipment, QC testing, sampling, TQM, GxP standards, and laboratory excellence.
  • Willingness to work in shifts.

Desirable Requirements

  • Degree in Pharmacy, Chemistry, or related field, with 0-4 years of experience.

Why Novartis: Join a community of passionate people working to help those with disease, fostering collaboration, support, and innovation. Learn more: Novartis Strategy & Culture

Join our Talent Network to stay connected and find suitable opportunities: Talent Network

Benefits and Rewards: Learn more in our Benefits & Rewards Handbook .

Additional Details

  • Seniority Level: Entry level
  • Employment Type: Full-time
  • Job Function: Quality Assurance
  • Industry: Pharmaceutical Manufacturing
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