REQ-10076176
Ápr 24, 2026
Singapore

Összegzés

Supports all GxP activities in the Quality department. Administers Quality Systems/ Processes including documentation, metrics and monitoring of actions and supports establishment of Quality operational processes.
-Performs routine GxP Compliance/ Operational activities according to Novartis Quality Standards. Supports Quality Projects and initiatives

About the Role

Major Accountabilities:

  • Maintains applicable Standard Operating Procedures (SOPs), GxP compliant documentation and records within the Novartis Quality Management System.
  • Ensures the integrity of all Quality Systems records and data, as applicable and collaboration of own team with other functions and departments -Ensures an adequate level of education, GxP knowledge .
  • Updates and maintains relevant information in electronic systems (e.g.Change Control, Documentation, Training).
  • Follow up and monitoring of e.g.CAPAs, actions, metrics, Quality plan).
  • Supports Quality Audits and Health Authority inspections.
  • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Minimum Requirement

  • Familiarity with Quality Management Systems is the pharmaceutical industry,
  • Familiarity/experience within a Good Manufacturing Practices (GMP) atmosphere
  • 1-2 years' experience in GMP documentation review, approval, and/or release would be ideal.

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

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

Development
Quality
Singapore
Mapletree Business City (MBC)
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.

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REQ-10076176

QA Associate

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