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Associate QC Scientist

WUXI XDC SINGAPORE PRIVATE LIMITED

Singapore

On-site

SGD 60,000 - 80,000

Full time

11 days ago

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Job summary

A leading company in the pharmaceutical sector in Singapore is seeking an Associate QC Scientist to conduct testing and ensure quality standards. The role involves performing complex tests, validating methods, and maintaining compliance with cGMP principles. Ideal candidates will possess a relevant degree and excel in analytical tasks.

Qualifications

  • Degree and above in relevant fields.
  • In-depth knowledge of cGMP principles.
  • Proficiency in English.

Responsibilities

  • Conduct various analytical and microbiological tests.
  • Assist in developing and validating testing methods.
  • Operate and maintain laboratory equipment.

Skills

Attention to detail
Troubleshooting
Quality-focused mindset

Education

Degree in pharmacy, chemistry, biochemistry, microbiology, analytical chemistry

Job description

Job Summary:
The Associate QC Scientist is responsible for conducting a range of testing and operational quality control activities.

Key Responsibilities:

  • Conduct various analytical, bioassay and microbiological tests, including CE-SDS, cIEF, cell-based potency assays, ELISA-based qualification, Karl Fischer titration, Total Organic Carbon (TOC) testing, UV-Vis spectrophotometry, FTIR, manual and automated titration, bioburden, sterility, container closure integrity testing (CCIT), and endotoxin testing.
  • Conduct utility related sampling at utility system and environmental monitoring at manufacturing facilities.
  • Assist in developing and validating analytical, bioassay and microbiological testing methods
  • Assist in analyzing and interpreting analytical, bioassay and microbiological results, maintaining accurate documentation.
  • Assist in investigating out-of-specification results and implementing corrective actions.
  • Operate and maintain laboratory equipment and instruments.
  • Manage in-process, release stability sample, and reference standards

Qualifications:

  • Degree and above in pharmacy, chemistry, biochemistry, microbiology, analytical chemistry, or related field.
  • Understanding of the drug development process preferred
  • In-depth knowledge of cGMP and compliance principles and a strong quality-focused mindset.
  • Strong attention to detail and ability to troubleshoot experimental challenges
  • Ability to work independently and as part of a collaborative team
  • Proficiency in English as a working language.
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