Analytical Lab Analyst I – QC & Method Validation

Lonza Group Ltd.

Singapore

On-site

SGD 42,000 - 68,000

Full time

41 hours ago
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Job summary

Lonza Singapore is seeking a Laboratory Analyst to perform diverse testing and analysis to support business requirements and ensure adherence to current Good Manufacturing Practices (cGMP).

You will engage in method development and transfers, record review, and equipment qualification while maintaining high standards of accuracy and safety. Lonza emphasizes ethical performance, teamwork, and meaningful impact on patient health worldwide.

Qualifications

  • Degree/Diploma in a relevant Science field or Equivalent.
  • Understanding and execution of spectroscopy and other assigned methods which may include chromatography methods (HPLC), Protein Concentration (A280 or SoloVPE).
  • Work experience preferably Lab experience in a biotech or medically related field
  • Good problem solving and analytical skills

Responsibilities

  • Prioritize and perform testing/analysis in a timely manner to support business requirements.
  • Analyze final product, in-process, and raw materials according to SOPs and test methods.
  • Document and review results in accordance with cGMP.
  • Troubleshoot analytical methods and equipment.
  • Involve in method transfers and validation.
  • Involved in equipment qualification and QC equipment selection.
  • Do assay trend analysis and document revisions.
  • Provide general lab support including housekeeping, equipment maintenance, inventory, and glassware management.
  • Perform other duties as assigned by Supervisor/Manager

Skills

Analytical skills
Problem solving
Lab experience
Chromatography techniques
HPLC
Spectroscopy

Education

Degree/Diploma in a relevant Science field

Tools

HPLC
Protein concentration (A280/SoloVPE)
Spectroscopy

Job description

Lonza Singapore is seeking a Laboratory Analyst to perform diverse testing and analysis to support business requirements and ensure adherence to current Good Manufacturing Practices (cGMP).

You will engage in method development and transfers, record review, and equipment qualification while maintaining high standards of accuracy and safety. Lonza emphasizes ethical performance, teamwork, and meaningful impact on patient health worldwide.

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