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Open nowPosted 31 days ago

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

MyCareersFuture94,028 open roles

Pay
SGD 2,800 – SGD 4,500 a month
Where
Central, Singapore
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Your applicationOpen nowQuality Associate (ELISA) (6 months | Maternity Cover) | Pharma MNC | WestMyCareersFuture · Central, Singapore

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The clock on this job

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7.8% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
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  2. 3.4%3 days
  3. 7.8%7 days
  4. 14.3%14 days
  5. 33.7%30 days
This job: posted 31 days ago

The posting

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; [email protected]

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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