QC Lab Analyst – GMP/ISO 17025, Chemistry

PT. Blue Ocean Labs; Batam; On-site; IDR 66,960,000 - 133,920,000; Full time

Job summary

PT. Blue Ocean Labs in Batam, Indonesia seeks a Laboratory Analyst / QC Analyst to perform chemical and instrumental analyses (GC FID) on raw materials, in-process and finished products.

You will maintain instruments, log data, and draft Certificates of Analysis (CoA) while ensuring GLP/ISO 17025 and GMP compliance. The ideal candidate holds a Diploma or BSc in a related science, with QC experience, strong English skills, and attention to detail.

Qualifications

• Diploma or Bachelor’s degree in a relevant science field.
• Quality Control experience is preferred.
• Strong knowledge of GLP, ISO 17025, ISO 9001, and GMP.
• Fluent English to read manuals and CoAs.

Responsibilities

• Perform routine laboratory analysis for chemical and instrumental testing (GC FID) on raw materials, in-process and finished goods.
• Perform routine verification, maintenance, and basic troubleshooting of laboratory analytical instruments.
• Record raw testing data and results in lab logbooks or system software.
• Prepare and draft Certificates of Analysis (CoA).
• Prepare, standardize, and label chemical reagents, volumetric solutions, and secondary reference standards with precise expiry tracking.
• Perform routine cleaning, basic maintenance, and daily verification/checking of analytical instruments and glassware.
• Maintain cleanliness, orderliness, and safety (5S) in the laboratory area.

Skills

GLP

ISO 17025

ISO 9001

GMP standards

Analytical thinking

Attention to detail

Fluent English

Education

Diploma (D3) or Bachelor’s Degree in Chemistry, Chemical Engineering, Pharmacy, Industrial Chemistry or related science

Quality Control experience preferred

Tools

GC FID

Job description

PT. Blue Ocean Labs in Batam, Indonesia seeks a Laboratory Analyst / QC Analyst to perform chemical and instrumental analyses (GC FID) on raw materials, in-process and finished products.

You will maintain instruments, log data, and draft Certificates of Analysis (CoA) while ensuring GLP/ISO 17025 and GMP compliance. The ideal candidate holds a Diploma or BSc in a related science, with QC experience, strong English skills, and attention to detail.