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QA Inspector Staff

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Onsite

QA Inspector Staff

PT Taisho Pharmaceutical Indonesia Tbk.

QA Inspector Staff

Skills

Testing & QACompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Depok, Depok City, West Java, Indonesia

Work mode:

Onsite

Published on:

3 September 2026

What they need


QA Inspector Staff

Implement GMP guidelines, review product batch records, and support quality-related business activities within the manufacturing site.

Accountabilities

  • Ensure SOPs are implemented in compliance with GMP requirements across daily GMP activities at the manufacturing site.
  • Ensure the site is adequately prepared for internal and external audits.
  • Review finished product batch documentation, including manufacturing and packaging records and product inspection results, before product release.
  • Monitor manufacturing processes according to the established schedule.
  • Conduct GMP-related training for production personnel and support investigations of deviations/events related to GMP activities.
  • Ensure the availability of required documents for product manufacturing, packaging, and testing activities.
  • Perform random sampling for specific deviation-related cases.

Education Requirements
Bachelor’s degree in pharmacy.

Experience Requirements

  • Have at least 1 year of experience as a QA Inspector in the pharmaceutical industry.
  • Proficient in chemical testing and instrumental analysis.
  • Have a good understanding of GMP
  • Have a good command of the computer
  • Good English skills, both verbal & written

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