Senior Technician, Quality Control (Contract 4 months)

Duopharma Biotech; Klang City; On-site; MYR 100,000 - 150,000; Full time

Job summary

A leading pharmaceutical company in Klang City is seeking a Senior Technician, Quality Control for a 4-month contract. The role involves conducting analytical testing on In-Process Quality Control and Finished Product samples, ensuring timely reporting and compliance with GLP, cGMP, and PIC/S standards. The ideal candidate should have a degree in a related field and relevant experience, with fresh graduates encouraged to apply. This position requires strong analytical skills and attention to detail.

Qualifications

• Minimum 1 year of working experience in a pharmaceutical or regulated manufacturing environment.
• Fresh graduates are welcome to apply.
• Knowledge of GLP, cGMP, and pharmaceutical quality systems.

Responsibilities

• Perform analysis on IPQC and Finished Product samples for product release.
• Ensure laboratory activities comply with GLP, cGMP, and PIC/S guidelines.
• Maintain accurate laboratory documentation.

Skills

Analytical skills

Attention to detail

Communication skills

Teamwork

Education

Degree in Pharmaceutical Technology, Chemistry or related discipline

Tools

HPLC

IR spectrophotometers

UV-Vis spectrophotometers

Job description

Senior Technician, Quality Control (Contract 4 months)

To conduct analytical testing on In-Process Quality Control (IPQC) and Finished Product samples in the Chemical Quality Control Laboratory, ensuring timely testing, accurate reporting, and compliance with GLP, cGMP, PIC/S, and company quality requirements.

The position is a contract for 4 months

Job Purpose

To conduct analytical testing on In-Process Quality Control (IPQC) and Finished Product samples in the Chemical Quality Control Laboratory, ensuring timely testing, accurate reporting, and compliance with GLP, cGMP, PIC/S, and company quality requirements.

The position is a contract for 4 months

Key Responsibilities

• Perform analysis on IPQC and Finished Product samples to support timely product release for local and export markets.

• Carry out routine and complex analytical tests including assay, identification, physical tests, and related substances testing.

• Ensure laboratory activities are conducted in compliance with GLP, cGMP, and PIC/S guidelines.

• Maintain accurate laboratory documentation, including test records and instrument logbooks.

• Assist in Phase 1a and Phase 1b laboratory investigations when required.

• Support analytical testing schedules to meet laboratory turnaround timelines.

• Review non-critical analytical reports when assigned by the superior.

• Perform column verification to ensure suitability for analytical use.

• Assist in preparing trend analysis reports as required.

• Perform calibration of Secondary Working Standards according to the approved schedule.

• Support inventory control, stock checks, and laboratory housekeeping activities.

• Assist in audit preparation and support investigation of audit findings.

• Maintain laboratory cleanliness and safety in accordance with company safety policies and OSHA guidelines.

Job Requirements

• Degree in Pharmaceutical Technology, Chemistry or related science discipline.

• Minimum 1 year of working experience in a pharmaceutical or regulated manufacturing environment.

• Fresh graduates are welcome to apply.

• Knowledge of GLP, cGMP, and pharmaceutical quality systems.

• Hands-on experience operating QC laboratory instruments such as HPLC, IR, and UV-Vis spectrophotometers.

• Strong analytical skills with good attention to detail.

• Good communication skills and ability to work effectively within a team.

• Demonstrates integrity, responsibility, and adherence to company values.

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