QC Analyst

Overview

Responsible for performing analysis of finished product and raw material to ensure compliance with the quality procedures and standard requirements.

Responsibilities

• Responsible for conducting testing based on a valid document and also reporting.
• Responsible for maintaining the availability of all reagents, reference standards, and spare parts by filling the stock card.
• Responsible for maintenance and monitoring of laboratory instruments and glassware.
• Responsible for sample handling at the laboratory.
• Responsible for filling QC performance, log book instrument, trend data, and stability data.
• Responsible for conducting method validation and cleaning validation based on protocol, and also prepared the report.
• Actively participating in Small Group Activities (SGA) and the Environment Health and Safety (EHS).

Education Requirements

Experience Requirements

About Taisho Pharmaceutical Indonesia

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).

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