QC Analyst

Sunward Pharmaceutical; Johor Bahru; On-site; MYR 39,000 - 58,000; Full time

Job summary

Sunward Pharmaceutical in Johor Bahru is seeking a Quality Control Analyst to ensure safe, contaminant-free products. You will perform routine analyses, operate HPLC and analytical instruments, and maintain GLP standards across raw materials, in-process, and finished products.

The position welcomes candidates with a certificate/diploma in science or pharmaceutical fields, supports rotation shifts and overtime, and emphasizes meticulous documentation and calibration of lab equipment.

Qualifications

• Education: Minimum Certificate/Diploma in Science or Pharmaceutical or equivalent.
• Fresh graduates are welcome to apply.
• Able to work on rotation shift and overtime.

Responsibilities

• Work closely with Microbiologist, Production, QC, and QA to prevent contamination.
• Routine analysis and recording of raw materials, intermediates and finished products.
• Operate HPLC and laboratory analytical instruments.
• Carry out stability testing.
• Carry out dissolution profile testing and monitoring.
• Carry out analytical method validation.
• Sampling and recording of packaging material.
• In-process granules and tablet line checks and recording.
• In-process syrup and cream checks.
• Approve packing processes.
• Calibrate/verify laboratory equipment and apparatus.
• Quality control check on raw material dispensing.
• Ensure labels and barcodes are complete and accurate.
• Prepare and record reagents and chemicals.
• Support working standard preparation and analysis.
• Maintain cleanliness of laboratory equipment and workspace.
• Practice GLP and lab safety.
• Maintain QC documents and equipment logs.

Skills

HPLC operation

Analytical instruments

GLP awareness

Quality control

Laboratory safety

Education

Certificate/Diploma in Science or Pharmaceutical

Tools

Calibration instruments

Job description

To work closely with Microbiologist, Production, QC personnel and QA department to ensure all apparatus and end products are safe and free from any contamination.

Routine analysis and recording of raw material, intermediates and finished product.

Operation of High Performance Liquid Chromatography (HPLC) and laboratory analytical instrument.

Carry out stability testing.

Carry out dissolution profile test and monitoring.

Carry out Analytical method validation.

Sampling, routine checking and recording of packaging material.

On line checking and recording of in-process granules and tablet

Checking and recording of in-process syrup, cream.

Checking and approval of packing process.

Carry out calibration/ performance verification of laboratory equipment/ Apparatus.

Quality Control check on raw material dispensing.

Ensure coding of labels and bar code labels are complete & accurate.

Preparation and recording of reagents and chemicals.

Perform analysis and support for working standard preparation.

Maintain tidiness and cleanliness of laboratory equipment and workplace.

Practice Good Laboratory Practice (GLP) and laboratory safety.

Maintain QC document in laboratory to ensure up to date and accurate.

Update laboratory equipment log book / Quality Control (QC) record book and all other QC documents.

1. Education: Minimum Certificate/Diploma in Science or Pharmaceutical or equivalent.

2. Qualified candidates with no working experience are welcomed to apply.

3. Able to work on rotation Shift and working overtime