Quality Associate (ELISA) (6 months - Maternity Cover) - Pharma MNC - West

GMP TECHNOLOGIES (S) PTE LTD; Singapore; On-site; SGD 42,000 - 60,000; Full time

Job summary

GMP Technologies (S) Pte Ltd is seeking an QC Laboratory Technician to perform routine chemistry and biochemistry testing on raw materials, in-process samples, utilities and finished products. You will support daily QC operations and maintain lab documentation to ensure timely testing and regulatory compliance.

The role requires a Diploma or Bachelor’s degree in Chemistry or related fields, GMP exposure, and strong analytical and communication skills.

Qualifications

• Diploma or Bachelor's degree in Chemistry, Biochemistry, Life Sciences or a related discipline.
• Experience in a GMP-regulated QC laboratory is preferred.
• Knowledge of chemistry and/or biochemistry laboratory testing.
• Familiarity with laboratory equipment, calibration and basic troubleshooting.
• Understanding of GMP, GLP and regulatory compliance requirements.
• Experience with laboratory documentation, SOPs and good documentation practices (GDP).
• Exposure to OOS, OOT, deviation investigations and CAPA is an advantage.
• Able to follow laboratory safety procedures and quality standards.
• Good analytical, problem-solving and communication skills.
• Able to work independently and as part of a team.
• Willing to provide occasional weekend or after-hours support when required

Responsibilities

• Perform routine chemistry and biochemistry testing on raw materials, in-process samples, utilities, environmental monitoring and finished products.
• Support daily QC laboratory operations to ensure timely testing.
• Prepare, review and maintain QC documents (e.g. SOPs, test records and work instructions).
• Maintain laboratory inventory, reagents and testing materials.
• Follow laboratory safety, GMP and regulatory requirements.
• Support reagent and analytical method qualification, verification and validation activities.
• Perform basic troubleshooting, calibration and maintenance of laboratory equipment.
• Coordinate equipment servicing and support qualification activities when required.
• Assist in laboratory investigations for OOS, OOT, deviations and equipment-related issues.
• Support CAPA implementation and root cause investigations.
• Participate in inspection readiness and regulatory compliance activities.
• Contribute to continuous improvement projects to enhance QC efficiency and quality.

Skills

Analytical skills

Problem-solving

Communication skills

Teamwork

Independent work

Education

Chemistry/Biochemistry degree

Tools

Laboratory equipment

Calibration

GDP (Good Documentation Practices)

Job description

Jobscope

• Perform routine chemistry and biochemistry testing on raw materials, in-process samples, utilities, environmental monitoring and finished products.
• Support daily QC laboratory operations to ensure timely testing.
• Prepare, review and maintain QC documents (e.g. SOPs, test records and work instructions).
• Maintain laboratory inventory, reagents and testing materials.
• Follow laboratory safety, GMP and regulatory requirements.
• Support reagent and analytical method qualification, verification and validation activities.
• Perform basic troubleshooting, calibration and maintenance of laboratory equipment.
• Coordinate equipment servicing and support qualification activities when required.
• Assist in laboratory investigations for OOS, OOT, deviations and equipment-related issues.
• Support CAPA implementation and root cause investigations.
• Participate in inspection readiness and regulatory compliance activities.
• Contribute to continuous improvement projects to enhance QC efficiency and quality.

Requirements

• Diploma or Bachelor's degree in Chemistry, Biochemistry, Life Sciences or a related discipline.
• Experience in a GMP-regulated QC laboratory is preferred.
• Knowledge of chemistry and/or biochemistry laboratory testing.
• Familiarity with laboratory equipment, calibration and basic troubleshooting.
• Understanding of GMP, GLP and regulatory compliance requirements.
• Experience with laboratory documentation, SOPs and good documentation practices (GDP).
• Exposure to OOS, OOT, deviation investigations and CAPA is an advantage.
• Able to follow laboratory safety procedures and quality standards.
• Good analytical, problem-solving and communication skills.
• Able to work independently and as part of a team.
• Willing to provide occasional weekend or after-hours support when required

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239