Shift QA Operations Technician I West, Pharma #HJN

Recruit Express Pte Ltd; Singapore; On-site; SGD 28,000 - 45,000; Full time

Job summary

Recruit Express Pte Ltd is seeking a quality professional to review and verify manufacturing and quality documentation to ensure compliance with procedures and standards.

The role involves GMP compliance, QA/QC, CAPA support, and collaboration with cross-functional teams to drive process improvements in a manufacturing environment in Singapore.

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 to ensure compliance with procedures and quality standards.
• Conduct quality inspections and routine 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 operations.
• Assist in investigating quality issues, deviations and customer complaints; support CAPAs.
• Collaborate with cross-functional teams to identify process improvements and maintain quality standards.
• Ensure GMP, GMP/QMS and workplace safety compliance.
• Perform other quality-related duties as assigned.

Education

Min NITEC / Diploma or equivalent in Life Sciences, Biotechnology, Pharmaceutical Science, Chemistry or Engineering

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.