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QC Technician

VWR Singapore Pte Ltd

Singapore

On-site

SGD 40,000 - 60,000

Full time

Today
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Job summary

A leading quality control firm in Singapore seeks a Quality Control Specialist to ensure compliance with quality standards through inspection and testing of materials and products. Candidates should possess a Diploma or Bachelor's degree in Chemistry, Microbiology, or a related field and have 1-2 years of relevant laboratory experience. This role involves maintaining laboratory compliance and detailed reporting in a team-focused environment.

Qualifications

  • Formal training in laboratory practices and GMP/GLP standards preferred.
  • Minimum 1-2 years experience in a Quality Control laboratory.
  • Familiarity with LIMS and environmental monitoring desirable.

Responsibilities

  • Conduct inspection and testing of products for quality compliance.
  • Develop and enforce quality control procedures.
  • Document inspection results accurately in LIMS.

Skills

Analytical techniques
Problem solving
Communication skills
Team collaboration
PPE usage

Education

Diploma or Bachelor's degree in Chemistry, Microbiology, Biotechnology or related discipline

Tools

Laboratory instruments
LIMS
Microsoft Office Suite
Job description
Responsibilities
  • Conduct inspection and testing of raw materials, in-process products, and finished goods to ensure compliance with quality standards.
  • Develop, implement, and enforce quality control procedures and standards.
  • Document inspection results, test data, and quality reports accurately and promptly.
  • Escalate /inform any issues pertaining to quality to QC supervisor
  • Maintain laboratory inventory using KANBAN systems for chemicals and consumables.
  • Preparation of test samples to be sent to contract laboratory for non-routine chemical and microbiological analyses of finished products.
  • Handle chemical waste disposal
  • Managing Retain samples chain of custody (e.g. Retrieval and storage)
  • Operate laboratory instruments (e.g., pH meter, conductivity meter, UV spectrophotometer, Karl Fischer titrator, FTIR, titration apparatus) in accordance with SOPs.
  • Follow established test methods and compendial standards (USP, EP, BP, JP, ACS) and EXCIPACT guidelines.
  • Analyze test results, calculate data, and prepare reports to verify compliance with specifications.
  • Perform Internal equipment Calibration or performance check.
  • Record final results and raw data in the Laboratory Information Management System (LIMS), if any
  • Handle hazardous materials in compliance with safety protocols and using appropriate PPE.
  • Complete documentation for accuracy, completeness, and legibility.
  • Any other adhoc assignment by QC supervisor
Requirements
  • Diploma or Bachelor's degree in Chemistry, Microbiology, Biotechnology, or a related scientific discipline including ITE Certificate or Higher Nitec in Chemical Process Technology, Biotechnology, Environmental Science, or a related discipline.
  • Formal training in laboratory practices, analytical techniques, and GMP/GLP standards is preferred.
  • Minimum 1-2 years of hands-on experience in a Quality Control laboratory within the pharmaceutical, chemical, or life sciences industry.
  • Experience with compendial testing (USP, EP, BP, JP) and working in cleanroom environments is an advantage.
  • Familiarity with LIMS, environmental monitoring, and equipment calibration is desirable.
  • Certification in Good Laboratory Practices (GLP), ISO standards (e.g., ISO 9001, ISO 17025), or EXCiPACT is a plus.
  • Safety training for handling hazardous materials and PPE usage is required
  • Applied working knowledge of various laboratory instrumentation
  • Ability to work collaboratively in a diverse team environment with people at all levels in the organization
  • Proficiency in Microsoft Word, Power Point, Excel and Access
  • Strong problem solving and analytical skills
  • Ability to communicate effectively, both verbally and in writing
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