QC Supervisor - GMP/GLP Analytical Lead

PT Taisho Pharmaceutical Indonesia Tbk.; Depok; On-site; IDR 290,160,000 - 513,360,000; Full time

Job summary

PT Taisho Pharmaceutical Indonesia Tbk. seeks a QC professional to supervise analysis of in-process, finished products and raw materials, ensuring GMP, GLP, and EHS compliance.

Requirements: Bachelor’s degree in Pharmacy with at least 5 years in pharmaceutical quality control; strong chemical testing and instrumental analysis skills; good English and computer proficiency. Responsibilities include coordinating analyses, supporting material releases with the QC APJ, sampling, maintaining QC

Qualifications

• Bachelor’s degree in Pharmacy required.
• Minimum 5 years in pharmaceutical quality control.
• Proficient in chemical testing, instrumental analysis, and English.
• Good computer skills.

Responsibilities

• Coordinate analyses of in-process, finished products and raw materials; ensure GMP, GLP, and EHS compliance.
• Schedule analyses and support for material releases with the QC APJ; manage sampling.
• Maintain QC documentation and supervise QC staff; conduct OOS investigations; ensure GLP training.

Skills

Chemical testing

Instrumental analysis

English language

Computer skills

Education

Bachelor's degree in Pharmacy

Job description

PT Taisho Pharmaceutical Indonesia Tbk. seeks a QC professional to supervise analysis of in-process, finished products and raw materials, ensuring GMP, GLP, and EHS compliance.

Requirements: Bachelor’s degree in Pharmacy with at least 5 years in pharmaceutical quality control; strong chemical testing and instrumental analysis skills; good English and computer proficiency. Responsibilities include coordinating analyses, supporting material releases with the QC APJ, sampling, maintaining QC