Editorial summary

The company is seeking a Quality Associate for a six-month maternity cover position in the pharmaceutical sector at their West location, offering a salary of 4,500. The role involves performing routine chemistry and biochemistry testing on raw materials, in-process samples, utilities, environmental monitoring, and finished products, while supporting daily QC laboratory operations. Key responsibilities include preparing and reviewing QC documents, maintaining laboratory inventory, and ensuring compliance with safety, GMP, and regulatory standards. The ideal candidate will have experience in laboratory testing, troubleshooting, calibration, and method validation within a regulated environment.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job id 23321 first appeared in Job-Q.com on 03 Aug 2026]

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

To find out more about this opportunity, please contact Fiona Koh;

We regret that only shortlisted candidates will be notified.

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

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