QA Inspector

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

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.

Bachelor’s degree in pharmacy.

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

Your application will include the following questions:

• Which of the following statements best describes your right to work in Indonesia?
• How many years' experience do you have as a Quality Assurance Inspector?
• Which of the following types of qualifications do you have?
• How would you rate your English language skills?

Pharmaceuticals, Biotechnology & Medical Devices 101-1,000 employees

Taisho Pharmaceutical Indonesia is the subsidiary of Taisho Pharmaceutical Co., Ltd., Japan - the number one over-the-counter medications company in Japan.

In Indonesia, Taisho Pharmaceutical has been operating since the end of 2009 after acquiring Bristol-Myers Squibb. Our main brands are Counterpain, Tempra, Theragran-M, Kenacort, Myco-Z and Mycostatin OS (Oral Suspension).