QC Technician

VWR SINGAPORE PTE. LTD.; Singapore; On-site; SGD 47,000 - 60,000; Full time

Job summary

VWR SINGAPORE PTE. LTD. is seeking a Quality Control Laboratory professional in Singapore to conduct inspection and testing of raw materials and finished products, ensuring compliance with quality standards.

The role involves developing, implementing, and enforcing QC procedures, with attention to accurate documentation and reporting. Responsibilities include instrument operation, adherence to compendial standards, data analysis, and SAP data entry, while maintaining inventory and supporting

Qualifications

• Formal training in laboratory practices, analytical techniques, and GMP/GLP standards is preferred.
• Diploma or equivalent required for the role.
• 2–3 years hands-on QC/Lab experience in pharma, chemical, or life sciences industries preferred.

Responsibilities

• Inspect raw materials and finished goods to ensure compliance with quality standards.
• Develop, implement, and enforce QC procedures and standards.
• Document inspection results, test data, and quality reports accurately and promptly.
• Identify quality issues with escalation to direct reporting.
• Maintain laboratory inventory using KANBAN systems for chemicals and consumables.
• Perform routine and non-routine chemical testing on materials and finished products.
• Operate laboratory instruments in accordance with SOPs.
• Follow test methods and compendial standards (USP, EP, BP, JP, ACS) and EXCiPACT guidelines.
• Analyze test results, calculate data, and prepare reports to verify compliance with specifications.
• Record final results and raw data in the SAP system.
• Support investigations, customer complaints, and troubleshooting activities.

Skills

GMP/GLP knowledge

Quality control experience

Analytical techniques

Education

Diploma in Chemistry, Microbiology, Biotechnology, or related

ITE/Higher Nitec in Chemical Process Technology, Biotechnology, Environmental Science, or related

Tools

SAP

Calibration procedures

Job description

Key Responsibilities

• Conduct inspection and testing of raw materials and finished goods to ensure compliance with quality standards.

• Develop, implement, and enforce quality control procedures and standards.

• Document inspection results, test data, and quality reports accurately and promptly.

• Identify quality issues with escalation to direct reporting

• Maintain laboratory inventory using KANBAN systems for chemicals and consumables.

• Perform routine and non-routine chemical testing on raw materials and finished products.

• Operate laboratory instruments (e.g., pH meter, conductivity meter, UV spectrophotometer, Karl Fischer titrator, FTIR, titration apparatus) in accordance with SOPs.

• Follow established test methods and compendial standards (USP, EP, BP, JP, ACS) and EXCIPACT guidelines.

• Analyze test results, calculate data, and prepare reports to verify compliance with specifications.

• Review laboratory data forms, including water testing and direct measurement analyses.

• Arrange Calibrate, maintain, and troubleshoot laboratory equipment to ensure optimal performance.

• Record final results and raw data in the SAP system.

• Support investigations, customer complaints, and troubleshooting activities through detailed analytical review.

• Apply appropriate disposition labels to materials (e.g., accepted, rejected, quarantined).

• Handle hazardous materials in compliance with safety protocols and using appropriate PPE.

QUALIFICATIONS (Education/Training, Experience and Certifications)

• Diploma in Chemistry, Microbiology, Biotechnology, or a related scientific discipline_ /orITE Certificate or Higher Nitec in Chemical Process Technology, Biotechnology, Environmental Science, or a related discipline.

• Formal training in laboratory practices, analytical techniques, and GMP/GLP standards is preferred.

Experience

• Minimum 2–3 years of hands-on experience in a Quality Control laboratory within the pharmaceutical, chemical, or life sciences industry.

• Experience with compendial testing (USP, EP, BP, JP) and working in cleanroom environments is an advantage.

• Familiarity with SAP and equipment calibration is desirable.

Certifications

• Certification in Good Laboratory Practices (GLP), ISO standards (e.g., ISO 9001, ISO 17025), or EXCiPACT is a plus.

• Safety training for handling hazardous materials and PPE usage is required.