Career Opportunities

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Assistant QC Supervisor

Supervise day-to-day running of QC laboratory, including daily testing, monitoring laboratory operations and test turnaround time, performing test methods development and validation.

Key Roles and Responsibilities

  • Supervise day-to-day running of QC laboratory
  • Supervise daily testing, monitor laboratory operations and test turnaround time
  • Supervise and train QC staff
  • Perform test method development and validation
  • Prepare and revise SOP and other relevant quality control documents

Qualification and Experience

  • Higher Diploma or Degree holder in Chemistry, Analytical Chemistry, Biology, Pharmaceutical Studies or related discipline
  • Familiar with analytical instruments such as HPLC, UPLC, GC, ICP and IR
  • 3 years working experience or above in Pharmaceutical company or commercial  testing laboratory and 2 year experience at supervisory level
  • Initiative, organized, hard-working, strong leadership and problem solving skills
  • Less experience will be considered as Senior QC Technician

Other related:

Validation Engineer (Quality Executive)

Define and plan validation activities to meet the cGMP requirements, coordinate with end users and process owners to develop and execute validation protocols for manufacturing facilities, systems, process and/or software; analyze validation related issues, implement validation related event, Change Control and CAPA.

Regulatory Affairs Assistant / Officer

Support timely compilation and submission of dossiers for approval of product registration, change of particulars and renewal, communicate with Department of Health and respond to their queries, provide regulatory support to internal departments.

QC Technician

Sampling and testing of raw materials, packaging materials, purified water, in-process samples, finished products and stability studies samples, operation of laboratory equipment, assisting in laboratory equipment calibration, qualification and maintenance.