Quality Assurance Specialist I | GMP & Documentation

Recruit Express Pte Ltd; Singapore; On-site; SGD 33,000 - 61,000; Full time

Job summary

Recruit Express Pte Ltd in Singapore is seeking a Quality Assurance/Quality Control professional to review manufacturing and quality documentation, perform inspections in production areas including cleanrooms, and support batch record preparation. The role emphasizes ensuring GMP/GxP compliance and maintaining quality systems.

This position involves assisting with CAPA investigations, collaborating with cross-functional teams to sustain high standards, and ensuring workplace safety throughout

Qualifications

• Min NITEC, Diploma or equivalent qualification in Life Sciences, Biotechnology, Pharmaceutical Science, Chemistry or Engineering.
• Prior experience in Quality Assurance, Quality Control or manufacturing operations is an advantage.
• Knowledge of GMP, GxP documentation and quality management systems is preferred.

Responsibilities

• Review and verify manufacturing and quality documentation for compliance with procedures and standards.
• Conduct quality inspections and walkdowns in production areas, including cleanrooms.
• Manage quality documents, records and samples with proper filing and retention.
• Support batch record preparation, label printing and documentation management for manufacturing.
• Assist in investigating quality issues, deviations and customer complaints and support CAPA.
• Collaborate with cross-functional teams to identify process improvements and maintain quality standards.
• Ensure compliance with GMP, GxP and quality management systems and workplace safety requirements.
• Perform other quality-related duties as assigned.

Skills

Quality Assurance

Quality Control

Documentation management

CAPA investigations

GMP knowledge

Education

NITEC or Diploma in Life Sciences/Pharma/Engineering

Job description

Recruit Express Pte Ltd in Singapore is seeking a Quality Assurance/Quality Control professional to review manufacturing and quality documentation, perform inspections in production areas including cleanrooms, and support batch record preparation. The role emphasizes ensuring GMP/GxP compliance and maintaining quality systems.

This position involves assisting with CAPA investigations, collaborating with cross-functional teams to sustain high standards, and ensuring workplace safety throughout