Chemistry Lab Technician (Contract til Jun 2027) – GMP/QC

GMP Technologies; Singapore; On-site; SGD 33,000 - 47,000; Full time

Job summary

GMP Technologies in Singapore is recruiting a Chemistry Lab Technician on a contract until June 2027 to support pharmaceutical QA/QC testing in Tuas. You will perform routine and non-routine chemical testings for raw materials and process samples, ensuring ALCOA+ data integrity and adherence to cGMP, cGDP, and cGLP guidelines.

Responsibilities include equipment calibration and maintenance, document drafting, training, investigations (OOS/abnormal results), and supporting lean 5S initiatives.

Qualifications

• Diploma or Degree in Chemistry, Life Sciences, or related field.
• Experience in a pharmaceutical or biotech lab is preferred.
• Able to perform routine chemical testing on materials and process samples.
• Familiarity with GMP and data integrity concepts (ALCOA+).
• Ability to follow SOPs and complete accurate documentation.

Responsibilities

• Perform routine and non-routine chemical testings with good observation of ALCOA+, cGMP, cGDP and cGLP.
• Support testing for raw materials and process samples and ensure timely reporting.
• Ensure right-first-time test executions and documentation with schedule adherence.
• Assist in investigations (OOS issues, atypical results) and CAPAs.
• Maintain lab housekeeping, safety compliance, and proper waste disposal.
• Perform equipment maintenance, calibrations, and liaise with vendors as needed.
• Participate in 5S, GPS lean activities, and continuous improvement projects.

Skills

ALCOA+

GMP

Data integrity

Documentation

Education

Diploma or Degree in Chemistry or Life Sciences

Tools

TOC testing

Conductivity testing

Calibration equipment

Job description

GMP Technologies in Singapore is recruiting a Chemistry Lab Technician on a contract until June 2027 to support pharmaceutical QA/QC testing in Tuas. You will perform routine and non-routine chemical testings for raw materials and process samples, ensuring ALCOA+ data integrity and adherence to cGMP, cGDP, and cGLP guidelines.

Responsibilities include equipment calibration and maintenance, document drafting, training, investigations (OOS/abnormal results), and supporting lean 5S initiatives.