QC Analyst II: Precision Testing & GMP Compliance

Novartis; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical company in Singapore is seeking a Quality Associate to support activities within the Quality department. The role involves managing sample storage, analytical testing, and ensuring compliance with cGxP standards. Candidates should have a background in pharmacy or chemistry with up to four years of experience in a laboratory environment. The company emphasizes collaboration and offers a community-oriented workplace.

Qualifications

• Previous experience in a laboratory environment in the pharmaceutical industry preferred.
• Knowledge of TQM and related industry GxP standards is essential.
• Experience in GMP and HSE compliant processes.

Responsibilities

• Manage sample storage and analytical testing.
• Ensure compliance with cGxP and data integrity.
• Detect and report potential risks and propose solutions.

Skills

Laboratory equipment

Quality Control (QC) Testing

Quality Control Sampling

Breakthrough Analysis

Operational Excellence

Continuous Learning

Digital & Tech Savvy

Education

University degree in Pharmacy or Chemistry

Job description

A leading pharmaceutical company in Singapore is seeking a Quality Associate to support activities within the Quality department. The role involves managing sample storage, analytical testing, and ensuring compliance with cGxP standards. Candidates should have a background in pharmacy or chemistry with up to four years of experience in a laboratory environment. The company emphasizes collaboration and offers a community-oriented workplace.