Laboratory Analyst

PT. Blue Ocean Labs; Batam; On-site; IDR 55,800,000 - 83,700,000; Full time

Job summary

PT. Blue Ocean Labs is seeking a Laboratory Analyst / QC Analyst to conduct chemical and physical testing of raw materials, in-process samples, and finished products of e-liquids, nicotine pouches, and flavor capsule.

You will perform routine GC FID analysis, maintain instruments, draft CoAs, ensure GMP/GLP/ISO compliance, and document results with clarity. Shift work and strict attention to detail are essential to ensure production quality.

Qualifications

• Diploma or Bachelor's degree in Chemistry or related field.
• Knowledge of GLP, ISO 17025, ISO 9001 and GMP.
• Understanding QC documentation (SOP, CoA).
• Fluent English for manuals and CoA readings.
• Able to work in shifts.
• Strong analytical thinking and attention to detail.

Responsibilities

• Perform routine laboratory analysis for chemical and instrumental testing (GC FID) on materials and products.
• Verify, maintain, and troubleshoot laboratory instruments.
• Record data in lab logs or system software.
• Prepare Certificates of Analysis (CoA).
• Prepare and label reagents and standards with expiry tracking.
• Maintain lab cleanliness, orderliness, and safety (5S).
• Ensure quality documentation complies with GLP/ISO standards.

Skills

Analytical thinking

Attention to detail

English proficiency

Problem solving

Communication skills

Integrity

Objectivity

Shift work

Report writing

Quick thinking

Education

Diploma or Bachelor's degree in Chemistry or related science

Tools

GC FID

Job description

Position Introductory:

Laboratory Analyst / QC Analyst responsible to conduct the laboratoty analysis, chemical and physical testing of raw materials, in-process samples, and finished products of e-liquids, nicotine pouches, and flavor capsule

Responsibilities:

• Perform routine laboratory analysis for chemical, and instrumental testing (GC FID) on raw materials, In-Process and finish good.
• 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 glasswares
• Maintain cleanliness, orderliness, and safety (5S) in the laboratory area.

Requirements:

• Diploma (D3) or Bachelor's Degree (S1) in Chemistry, Chemical Engineering, Pharmacy, Industrial Chemistry, or a related scientific discipline.Prefer to have someone that experience as Quality Control
• Strong background in GLP, ISO 17025, ISO 9001, and GMP standards.
• Knowledge of chemical raw material specifications, organic solvents (PG/VG), aromatic compounds, and nicotine chemistry.
• Understanding of Quality Control documentation (SOP, Work Instructions, Certificate of Analysis / CoA)
• Strong analytical thinking and meticulous attention to detail.
• Fluent English proficiency for reading instrument manuals, SOPs, and raw material CoAs.
• Having capability to problem solving, effective communication, integrity and objectivity.
• Able to quick thinking and quick action to handle any issue related with the Quality in the production.
• Have analytical thinking to use as basic problem solving.
• Able to work by shift hour.
• High proficiency in filling out report with clear and objective language.