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.