Advanced Analytical Technician

2 weeks ago

Singapore beBeeQualityControl Full time $3,600 - $4,800
Job Title: Quality Control Specialist

We are seeking a highly skilled and detail-oriented Quality Control Specialist to join our team in the pharmaceutical industry. The successful candidate will be responsible for conducting quality control analyses, ensuring compliance with laboratory and analytical methods, cGMP, health, safety, and environmental standards.

Key Responsibilities:

  • Assist in carrying out on-the-job training of other quality control specialists, incorporating cGMP and safety procedures.
  • Perform and carry out analytical testing in compliance with specifications, analytical methods, laboratory methods, and pharmacopoeia requirements.
  • Monitor the calibration and maintenance program for laboratory instruments/equipment and ensure compliance with established schedules.
  • Assist in qualification of laboratory equipment and validation of analytical methods.
  • Ensure that analyses are carried out and reported in accordance with GLP (Good Laboratory Practices). Ensure that analyses are completed on time and are consistent with business requirements.
  • Conduct OOS and atypical results investigation.
  • Qualify, maintain, and calibrate laboratory equipment.
  • Report and trend test results.
  • Plan and assure cGMP compliant quality testing and documentation according to schedule.
  • Prepare laboratory reagents in compliance with GLP and laboratory SOP requirements.
  • Assist in preparation of standard operating procedures and documentation, as well as participate in departmental activities as required.
  • Maintain and develop all required laboratory documents (i.e., raw data sheets, log books).
  • Handle electronic raw data in compliance with regulations and guidelines.
  • Be prepared for inspections and audits related to cGMP and EHS issues.
  • Ensure safe working practices in the laboratory by practicing and communicating safety.

Requirements:

  • Preferably possess 1 year's hands-on analytical testing experience in a lab environment from the pharmaceutical industry.
  • Familiarity with analytical equipment (e.g., HPLC, GC, etc.).
  • Will to work shifts on a rotational basis.
  • Analytical, methodical, and quality-conscious mindset.
  • Good knowledge of FDA regulations and cGMP.
  • Preferably hold a Diploma in Chemistry/Chemical Process Technology/Bio-Process Technology or an ITE graduate.

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