Get more replies from employers
Send a job-specific resume in minutes.
Range Pharma Sdn. Bhd. in Malaysia is seeking a disciplined Lab Assistant to join the Quality Control department. You will conduct sampling, testing, and maintain laboratory standards to ensure product quality.
The role requires full-time work Monday to Friday, 8:30 AM to 6:00 PM; education: SPM/SVM; strong attention to detail and SOP compliance; opportunities to grow within QC and build career in pharma.
Jora Malaysia will close on 9th September 2026. Thank you for being with us, we are cheering you on as you continue your career journey.
We are seeking a disciplined and detail-oriented Lab Assistant to join our Quality Control department. You will play a vital role in ensuring our products meet the highest standards through rigorous sampling, testing, and laboratory maintenance.
Quality Inspection: Act as the key personnel for sampling and inspecting raw materials and packaging to ensure conformity to specifications.
Testing & Analysis: Perform final product checks and conduct in-process QC (e.g., pH measurements, loss on drying, solubility, and clarity).
Equipment Management: Handle routine verification and calibration of laboratory equipment to maintain accuracy.
Lab Operations: Manage laboratory housekeeping, including distilled water collection, cleaning apparatus, and chemical waste disposal.
Documentation: Prepare and compile test results, reports, and maintain QC retain sample rooms and log sheets.
Operational Support: Provide duty coverage for label printing and support the QC Head in achieving department targets.
Education: Minimum SPM / SVM graduate.
Skills: High attention to detail, disciplined in following SOPs, and comfortable working in a laboratory environment.
Attitude: Proactive, willing to learn, and able to work well within a technical team.
Availability: Must be able to work full-time (Monday – Friday, 8:30 AM – 6:00 PM).
A strategic role in a pharmaceutical manufacturing environment.
Opportunity to build a career pipeline within the QC department.