PT Taisho Pharmaceutical Indonesia Tbk.
QA Inspector Staff
Skills
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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