Gmp Technologies (S) Pte Ltd · MyCareersFuture · 1mo
Quality Associate (ELISA) (6 months | Maternity Cover) | Pharma MNC | West
Singapore, Central- Posted
- 2026-09-01 (1mo)
- Place
- Singapore, Central
- Commitment
- Contract
- Salary
- SGD 2,800 – 4,500 / month
- Experience
- 1+ YOE
- Education
- Diploma
- Department
- Engineering
- Source
- MyCareersFuture (the employer’s own listing)
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Skills in this posting
Pharmaceutical IndustryChemistryLaboratoryCalibrationLab EquipmentTroubleshootingContinuous ImprovementLaboratory Testing
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; fiona.koh@gmprecruit.com
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239
Gmp Technologies (S) Pte Ltd
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