QC Analyst

QC Analyst

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

Accountabilities

• 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

Vocational High School of Chemical Analyst

Experience Requirements

• Have a minimum of 1 year of experience in Quality Control in the Pharmaceutical industry.

• Have a good understanding of the basic principles of Good Laboratory Practice and Data Integrity

• Have a good command of the computer

• Experience in the pharmaceutical industry is preferable

Information :

• Company : Taisho Pharmaceutical Indonesia
• Position : QC Analyst
• Location : Depok
• Country : ID