Manufacturing Quality Technician I SHIFT, West, Pharma #HJN

Recruit Express Pte Ltd; Singapore; On-site; SGD 39,000 - 58,000; Full time

Job summary

Recruit Express Pte Ltd in Singapore is seeking a Quality Assurance professional to review manufacturing and quality documentation, ensuring adherence to SOPs and GMP standards. The role includes inspections in production areas, including cleanrooms, plus handling batch records and documents.

You will support CAPA activities, investigate quality issues, and collaborate with cross-functional teams to drive process improvements and maintain safety and quality throughout operations.

Qualifications

• Min NITEC, Diploma or equivalent 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 to ensure compliance with procedures and quality standards.
• Conduct quality inspections and routine walkdowns in production areas, including cleanroom environments.
• Manage quality documents, records and samples, ensuring proper documentation, filing and retention.
• Support manufacturing operations through batch record preparation, label printing and documentation management.
• 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, quality management systems and workplace safety requirements.
• Perform other quality-related duties as assigned.

Skills

Quality Assurance

Documentation control

GMP knowledge

Cross-functional collaboration

Education

Diploma or equivalent

Job description

Duties:
Review and verify manufacturing and quality documentation to ensure compliance with established procedures and quality standards.

Conduct quality inspections and routine walkdowns in production areas, including cleanroom environments.

Manage quality documents, records and samples, ensuring proper documentation, filing and retention.

Support manufacturing operations through batch record preparation, label printing and documentation management.

Assist in investigating quality issues, deviations and customer complaints, and support corrective and preventive actions (CAPA).

Collaborate with cross-functional teams to identify process improvements and maintain quality standards.

Ensure compliance with Good Manufacturing Practices (GMP), quality management systems and workplace safety requirements.

Perform other quality-related duties as assigned.

Job Requirements

• Min NITEC, Diploma or equivalent qualification in a relevant discipline, such as 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.