QC Lab Technician

Opto-Pharm Pte Ltd; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A pharmaceutical company in Singapore is seeking a detail-oriented QC Technician to support the QC Manager in conducting quality checks for raw materials and finished goods. The role requires maintaining quality documentation and ensuring compliance with GMP. Applicants should have a relevant diploma or degree, attention to detail, and the ability to work rotating shifts. This is a crucial position to uphold product quality standards.

Qualifications

• Diploma or degree in a relevant field is required.
• Ability to work rotating shifts including night shifts.
• Knowledge of laboratory quality control processes is preferred.

Responsibilities

• Conduct inspection and testing of incoming raw materials, WIPs, and finished products.
• Prepare test solutions and materials for laboratory use.
• Maintain quality documentation and ensure compliance with quality manuals.

Skills

Attention to detail

Teamwork

Communication skills

Knowledge of GMP

Education

Diploma in Chemical Process Technology or Pharmaceutical Science

Degree in Chemistry/Quality Assurance

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 rotating shifts (4-day work week including night shifts).
• Strong attention to detail and commitment to product quality.
• Good teamwork and communication skills.
• Knowledge of GMP and quality control processes preferred.