QC Lab Technician

OPTO-PHARM PTE LTD; Singapore; On-site; SGD 36,000 - 48,000; Full time

Job summary

OPTO-PHARM PTE LTD in Singapore is seeking a detail-oriented QC Technician to support the QC Manager with quality checks for raw materials, in-process samples, and finished goods.

You will maintain quality documentation, assist in CAPA and audits, and help ensure GMP compliance. The role requires a Diploma or Degree in relevant field and the ability to work 12-hour shifts, with strong teamwork and communication.

Qualifications

• Diploma in Chemical Process Technology, Pharmaceutical Science, Biotechnology, or Degree in Chemistry/Quality Assurance.
• Able to work 12-hour shifts.
• Strong attention to detail and commitment to product quality.
• Good teamwork and communication skills.
• Knowledge of GMP and quality control processes preferred.

Responsibilities

• Conduct inspection and testing of incoming raw materials, WIPs, and finished products.
• Retain and analyze finished product samples from production lines.
• Prepare test solutions, reagents, and other materials for laboratory use.
• Assist in failure analysis, CAPA, and customer complaint investigations.
• Maintain quality documentation and ensure compliance with SOPs and quality manuals.
• Support GMP audits, validation, qualification, and change control activities.
• Assist in maintaining Product Quality and Technical Files.
• Uphold GMP and ensure adherence to quality standards.

Skills

Detail-oriented

Teamwork

Communication skills

GMP knowledge

Education

Diploma / Degree in Chemistry or QA

Job description

Position Overview

We are looking for a detail-oriented and responsible QC Technician to support our QC Manager in conducting quality checks for all raw materials, in-process samples, and finished goods. This role also involves maintaining quality documentation and ensuring compliance with established product standards and GMP requirements.

Key Responsibilities

• Conduct inspection and testing of incoming raw materials, WIPs, and finished products.
• Retain and analyze finished product samples from production lines.
• Prepare test solutions, reagents, and other materials for laboratory use.
• Assist in failure analysis, corrective and preventive actions (CAPA), and customer complaint investigations.
• Maintain quality documentation and ensure compliance with company quality manuals and SOPs.
• Support GMP audits, validation, qualification, and change control activities.
• Assist in maintaining Product Quality and Technical Files.
• Uphold Good Manufacturing Practices (GMP) and ensure adherence to quality standards.

Requirements

• Diploma in Chemical Process Technology, Pharmaceutical Science, Biotechnology, or Degree in Chemistry/Quality Assurance.
• Able to work 12-hour shifts.
• Strong attention to detail and commitment to product quality.
• Good teamwork and communication skills.
• Knowledge of GMP and quality control processes preferred.