QC Supervisor - GMP/GLP Analytical Lead
Job in
44164, Depok, Indonesia
Listed on 2026-09-08
Listing for:
PT Taisho Pharmaceutical Indonesia Tbk.
Full Time
position Listed on 2026-09-08
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Job Description & How to Apply Below
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
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