Quality Control Supervisor

Opto-Pharm Pte Ltd; Singapore; On-site; SGD 48,000 - 65,000; Full time

Job summary

A pharmaceutical company in Singapore seeks a proactive QC Supervisor/Senior QC Officer to assist the QC Manager in overseeing quality control activities. This role involves supervising lab technicians, inspecting raw materials, and ensuring compliance with ISO 13485 and cGMP standards. Candidates should have a related diploma or degree and at least 3 years of relevant experience in quality control tasks.

Qualifications

• Minimum 3 years of relevant experience in quality control or related laboratory work.
• Strong knowledge of ISO 13485 and cGMP requirements.
• Able to supervise and motivate a team effectively.

Responsibilities

• Supervise and provide guidance to lab technicians in daily quality control activities.
• Inspect incoming raw materials for compliance with current standards.
• Conduct periodic checks and analyses on work-in-progress (WIP) and finished products.
• Prepare technical reports, testing standards, and specifications for processes and products.

Skills

Supervisory skills

Knowledge of ISO 13485

cGMP compliance

Good communication skills

Detail-oriented

Education

Diploma in Chemical Process Technology

Degree in Chemistry/Quality Assurance

Job description

Position Overview

We are looking for a proactive and experienced QC Supervisor / Senior QC Officer to assist the QC Manager in overseeing quality control activities, including the inspection of raw materials and finished goods, maintaining quality documentation, and supervising lab technicians. This role plays a key part in ensuring product reliability, regulatory compliance, and continuous quality improvement.

Key Responsibilities

• Supervise and provide guidance to lab technicians in daily quality control activities.
• Inspect incoming raw materials for compliance with current standards.
• Conduct periodic checks and analyses on work-in-progress (WIP) and finished products.
• Retain and test finished product samples to ensure quality consistency.
• Assist in failure analysis, corrective and preventive actions (CAPA), and responses to customer complaints.
• Support GMP audits, validation, qualification, and change control processes.
• Maintain and update Product Quality documentation and Technical Files.
• Prepare technical reports, testing standards, and specifications for processes and products.
• Ensure adherence to ISO 13485, cGMP, and good laboratory practices.

Requirements

• Diploma in Chemical Process Technology, Pharmaceutical Science, Biotechnology, or Degree in Chemistry/Quality Assurance.
• Minimum 3 years of relevant experience in quality control or related laboratory work.
• Strong knowledge of ISO 13485 and cGMP requirements.
• Able to supervise and motivate a team effectively.
• Good communication and interpersonal skills to work with multi-national staff.
• Detail-oriented, organized, and able to manage multiple priorities.