QA Inspector Staff

PT Taisho Pharmaceutical Indonesia Tbk.; Depok; On-site; IDR 60,000,000 - 100,000,000; Full time

Job summary

Taisho Pharmaceutical Indonesia Tbk. is seeking a QA Inspector to implement GMP guidelines at the manufacturing site, review batch records, and support quality-related activities.

You will monitor processes, assist audits, train production personnel, and ensure documents for manufacturing, packaging, and testing are ready, with at least 1 year of relevant experience.

Qualifications

• Bachelor’s degree in pharmacy is required.
• At least 1 year of experience as a QA Inspector in the pharmaceutical industry.
• Proficient in chemical testing and instrumental analysis.
• Good understanding of GMP principles.
• Good command of computers and software.

Responsibilities

• Implement GMP guidelines across daily activities at the manufacturing site.
• Review finished product batch documentation prior to release.
• Monitor manufacturing processes according to the schedule.
• Conduct GMP-related training for production personnel.
• Support investigations of GMP-related deviations/events.
• Ensure availability of documents for manufacturing, packaging, and testing activities.
• Perform random sampling for deviation-related cases.

Skills

GMP knowledge

Chemical testing

Instrumental analysis

Computer literacy

Education

Bachelor’s degree in pharmacy

Job description

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

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).