jobs in Duopharma Biotech Berhad

Duopharma Biotech Berhad Hiring! Full Time QC Senior Technician in Negeri Sembilan - Ricebowl

QC Senior Technician

Duopharma Biotech Berhad

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Working Location

  • Nilai Negeri Sembilan Malaysia

Job Description

Responsibilities

Company Description

Duopharma Biotech Berhad is one of Malaysia's leading pharmaceutical companies, with operations dating back to 1978 and listed on the Main Market of Bursa Malaysia. The company specializes in Manufacturing, R&D, and Commercialisation, offering over 300 generic medicines and several popular Consumer Healthcare brands such as CHAMPS, FLAVETTES, and UPHAMOL. As a pioneer in halal-certified pharmaceuticals, Duopharma Biotech ensures its products meet stringent quality and hygiene standards. Headquartered in Kuala Lumpur, the company operates manufacturing facilities in Selangor and has a growing presence in Indonesia, the Philippines, and Singapore. Committed to innovation and sustainability, Duopharma Biotech delivers smarter healthcare solutions to communities across Asia and beyond.

Role Description

This is a full-time, on-site role for a QC Senior Technician based in Bandar Baru Bangi. Key responsibilities include performing quality control tests on raw materials, in compliance with established standards and guidelines. The role also involves documenting and analyzing test results, and ensuring adherence to quality assurance policies. The QC Senior Technician will collaborate with cross-functional teams to supporting the continuous improvement of QC processes.

Qualifications

  • Proficiency in Quality Control and Quality Assurance practices
  • Strong Analytical Skills for evaluating data and ensuring product compliance
  • Experience with Laboratory Skills, including proper handling of samples and materials
  • Knowledge of Laboratory Equipment usage, calibration, and maintenance
  • Attention to detail and the ability to follow strict guidelines and protocols
  • Bachelor’s degree or diploma in Chemistry, Pharmaceutical Sciences, or related fields is preferred
  • Previous experience in a pharmaceutical or manufacturing environment is an advantage
  • Familiarity with regulatory standards such as GMP (Good Manufacturing Practice) is beneficial

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