QA Engineer (Tuas, Manufacturing)

RECRUIT EXPERT PTE. LTD.

Singapore

On-site

SGD 28,000 - 45,000

Full time

14 days+

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Job summary

RECRUIT EXPERT PTE. LTD. is seeking a QC/QA inspector to perform inspections on raw materials, in-process, and finished goods in a GMP/ISO-aligned environment in Singapore. You will conduct testing, document results, and help identify non-conformances while supporting corrective actions.

Ideal candidates have 2+ years in QC/QA within manufacturing or healthcare-related industries, with strong attention to detail and solid documentation practices for quality systems and calibration support.

Qualifications

  • NITEC in Chemistry, Engineering, or a related discipline.
  • At least 2 years of QC/QA experience, preferably within manufacturing, medical devices, pharmaceuticals, or healthcare-related industries.
  • Familiar with QC tools, testing methods, and quality systems.
  • Strong attention to detail and good documentation skills.
  • Comfortable working in a lab or production environment.

Responsibilities

  • Perform raw material, in-process, and finished goods inspections in accordance with QC standards and procedures.
  • Conduct testing, measurements, and documentation of results to ensure product quality and compliance.
  • Identify and report non-conformances, and assist in investigation and corrective actions.
  • Maintain proper documentation in line with quality systems (e.g., GMP, ISO standards).
  • Support calibration, housekeeping of lab equipment, and continuous improvement initiatives.

Skills

Quality control
Documentation
Lab techniques
Attention to detail
GMP/ISO awareness

Education

NITEC in Chemistry/Engineering

Tools

QC tools
Testing methods
Quality systems

Job description

  • Perform raw material, in-process, and finished goods inspections in accordance with QC standards and procedures.
  • Conduct testing, measurements, and documentation of results to ensure product quality and compliance.
  • Identify and report non-conformances, and assist in investigation and corrective actions.
  • Maintain proper documentation in line with quality systems (e.g., GMP, ISO standards).
  • Support calibration, housekeeping of lab equipment, and continuous improvement initiatives.

Requirements:

  • NITEC in Chemistry, Engineering, or a related discipline.
  • At least 2 years of QC/QA experience, preferably within manufacturing, medical devices, pharmaceuticals, or healthcare-related industries.
  • Familiar with QC tools, testing methods, and quality systems.
  • Strong attention to detail and good documentation skills.
  • Comfortable working in a lab or production environment.

EA Licence: 19C9701

Registration: R1326740

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