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QC Analyst III

3 weeks ago


Singapore Novartis Singapore Full time

Join to apply for the
QC Analyst III (Analytical)
role at
Novartis Singapore .
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:
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 are in compliance with cGxP, including data integrity
Stability testing and sample management (when not centralized)
Analytical documentation of stability samples to cGxP standards
HSE:
Comply with all HSE guidelines
Detect and report potential accidents, risks, and propose solutions
Participate in initial training and retraining
Essential Requirements:
Preferred: Previous experience in a pharmaceutical laboratory environment, including quality assurance, production, aseptic technique
Collaboration; result-oriented
Administrative activities aligned with GMP and HSE standards
Results-driven attitude including resilience and operational excellence
Knowledge of laboratory equipment, QC testing, sampling, TQM, GxP standards, and decision-making in quality
Willing to work in 12-hour rotational shifts
Desirable Requirements:
Completed apprenticeship as a laboratory assistant or equivalent training
Proficiency in English and local language (oral and written)
Why Novartis:
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Additional Details:
Seniority level: Entry level
Employment type: Full-time
Job function: Quality Assurance
Industries: Pharmaceutical Manufacturing
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