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Analyst, Quality Control

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Onsite

Analyst, Quality Control

Randstad – Lonza

Analyst, Quality Control

Skills

Compliance

2 months ago

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Important information


Contract type:

Permanent

Salary:

SGD 48,000 – SGD 66,000 / year

Work mode:

Onsite

Published on:

19 August 2026

What they need


The QC Analyst will be responsible for Biochemistry Area in the QC Lab to support Lot Release activities

What you’ll get

  • An agile career and dynamic working culture in a global life sciences leader.
  • An inclusive and ethical workplace that values diversity and integrity.
  • Competitive compensation programs that recognize high performance.
  • Professional growth opportunities through cross-functional projects and global exposure.
  • Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums.
  • Company transport provided from designated MRT locations to and from the Tuas site.
  • Access to Lonza’s full suite of employee benefits: www.lonza.com/careers/benefits
  • Willing to do 12hours Shift role

What you’ll do:

  • Prioritize and perform analytical testing to meet business timelines
  • Test final product, in-process, and stability samples per SOPs and methods
  • Document and review results in compliance with cGMP and data integrity requirements
  • Execute methods such as ELISA, PCR, CE, SDS-PAGE, IEF/icIEF, potency, and other physicochemical assays
  • Support general lab operations: housekeeping, equipment upkeep, inventory, autoclaving, and glassware management
  • Prepare and maintain standards/reagents based on GMP requirements
  • Troubleshoot analytical methods and equipment issues
  • Participate in equipment qualification and maintenance
  • Support or lead OOS and deviation investigations; draft reports
  • Train others on test methods
  • Contribute to method transfer and validation activities
  • Author change controls, test methods, and SOPs

What we’re looking for:

  • Degree or higher with 5 years of QC/Quality experience in biopharmaceuticals
  • Preferably lab experience in biotech or medically related fields
  • Familiarity with FDA, EMEA, ICH guidelines and GMP quality systems
  • Strong planning, prioritization, and documentation skills
  • Good communication and interpersonal abilities
  • Analytical, meticulous, and quality-focused mindset
  • Team player who can work independently with strong safety and timeline discipline
  • Openness to new challenges and continuous improvement

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