QC Lab Analyst – E-Liquid & Nicotine Products

YSQ International; Batam; Presencial; IDR 60.000.000 - 110.000.000; Jornada completa

Descripción de la vacante

YSQ International is seeking a Laboratory Analyst / QC Analyst to conduct chemical and physical testing on raw materials, in-process samples, and finished products such as e-liquids, nicotine pouches, and flavor capsules. Proficiency with GC FID and strict adherence to documentation is essential.

You will document results, prepare CoAs, standardize reagents, and maintain laboratory compliance with GLP, ISO 17025, ISO 9001, and GMP standards.

Formación

• Diploma or Bachelor's degree in chemistry or related field.
• Experience in Quality Control.
• Familiar with GLP, ISO 17025, ISO 9001, GMP.
• Knowledge of raw material specs and solvents.

Responsabilidades

• 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.

Conocimientos

Analytical thinking

Attention to detail

Problem solving

English proficiency

Integrity and objectivity

Shift work capable

Lab report writing

Educación

Diploma (D3) or Bachelor's Degree in Chemistry or related field

Herramientas

GC FID

Descripción del empleo

YSQ International is seeking a Laboratory Analyst / QC Analyst to conduct chemical and physical testing on raw materials, in-process samples, and finished products such as e-liquids, nicotine pouches, and flavor capsules. Proficiency with GC FID and strict adherence to documentation is essential.

You will document results, prepare CoAs, standardize reagents, and maintain laboratory compliance with GLP, ISO 17025, ISO 9001, and GMP standards.