Chemistry Lab Technician (Contract til Jun 2027) | Pharma | Tuas

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

Chemistry Lab Technician (Contract til Jun 2027) | Pharma | Tuas

Job Openings Chemistry Lab Technician (Contract til Jun 2027) | Pharma | Tuas

About the job Chemistry Lab Technician (Contract til Jun 2027) | Pharma | Tuas

Jobscope:

• Performs routine and non-routine testings in the following areas with good observation of ALCOA+, cGMP, cGDP and cGLP requirements:
• Chemical testings for raw materials and utilities samples (prefer TOC and conductivity experience)
• Chemical testings to support manufacturing processes, process validations, cleaning validations and reagent qualifications
• Ensures right-first-time test executions and documentation, with schedule adherence.
• Performs peer review for verification of task and data.
• Ensures training competencies are up-to-date and comply to global organizations training policies.
• Performs equipment troubleshooting, calibrations, maintenance and verifications as assigned. Initiates repair work requests and liaise with vendors as necessary.
• Identifies and reports issues (e.g. invalid results/OOS/atypical results/equipment failure) in QC to superintendent/manager in a timely manner. Participates in laboratory investigations (when required) and assist in timely closure of investigations and CAPAs.
• Assists in document drafting and periodic review (e.g. SOPs, OJTs, WRAs, CRAs, QMCs, control charts)
• Supports activities related to GPS (e.g. tiers, Gemba, DMAIC, 5S, standard work etc) for continuous improvement. Practises 5S and ensures good housekeeping of laboratory, work area and equipment. Also support lean activities and improvement projects with achievements.
• Takes initiative to ensure good inventory of QC materials and reagents (e.g. purchased chemicals and prepared materials / glassware) to support testing activities; ensures no overstocking of inventory
• Ensures inspection-readiness of the QC laboratories.
• Adheres to all safety and security policies and practices. Ensures wastes are disposed appropriately and promptly.

Requirements:

• Diploma or Degree in Chemistry, Life Sciences, or related field
• Some experience in a lab environment, preferably in pharmaceutical or biotech industry
• Able to perform routine chemical testing (raw materials, utilities, process samples)
• Experience with TOC and conductivity testing is an advantage
• Basic understanding of GMP and data integrity (ALCOA+)
• Able to follow SOPs and complete documentation accurately
• Support equipment maintenance, troubleshooting, and calibration when required
• Assist in investigations (e.g., OOS or abnormal results)
• Support method validation / verification activities when needed
• Maintain good housekeeping (5S) and lab organization
• Ensure safety compliance and proper waste disposal
• Willing to provide occasional weekend or off-hours support

We regret that only shortlisted candidates will be notified.

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This is in partnership with the Employment and Employability Institute Pte Ltd (e2i).

e2i is the empowering network for workers and employers seeking employment and employability solutions. e2i serves as a bridge between workers and employers, connecting with workers to offer job security through job-matching, career guidance and skills upgrading services, and partnering employers to address their manpower needs through recruitment, training, and job redesign solutions. e2i is a tripartite initiative of the National Trades Union Congress set up to support nation-wide manpower and skills upgrading initiatives.

By applying for this role, you consent to GMP Recruitment Services (S) Pte Ltds PDPA and e2is PDPA