Senior QC Associate, Projects — On‑Site Singapore

GSK

Singapore

On-site

SGD 60,000 - 90,000

Full time

14 days+
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Job summary

GSK in Singapore is seeking a Senior / QC Associate (Projects) to perform analytical testing, manage samples, and support project work ensuring compliance and timely manufacturing and laboratory activities.

You will collaborate with lab, production, and quality teams, document precisely, and contribute to method development and investigations. This role offers hands-on technical growth and opportunities to lead improvements in a GMP environment.

Qualifications

  • Diploma or degree in Chemistry, Biology, Biochemistry, Biotechnology or related life sciences.
  • Minimum of 2 years of laboratory experience in analytical or QC.
  • Practical knowledge of GLP/GxP and good documentation practices.
  • On-site work in Singapore.
  • Clear written and spoken English with accurate documentation.
  • Able to work independently and as part of a team and to follow shift patterns.

Responsibilities

  • Perform testing for project activities to meet quality and regulatory standards.
  • Manage sample receipt, triage, storage, chain of custody and disposition.
  • Support method development, verification, validation and transfer activities.
  • Operate and calibrate laboratory equipment; arrange maintenance with vendors.
  • Lead or support project tasks such as process improvements and documentation updates.
  • Maintain accurate records and follow documentation practices for inspection readiness.

Skills

Analytical testing
Documentation
Team collaboration
English proficiency

Education

Diploma or degree in Chemistry/Biology/Life sciences

Tools

LIMS
Excel

Job description

GSK in Singapore is seeking a Senior / QC Associate (Projects) to perform analytical testing, manage samples, and support project work ensuring compliance and timely manufacturing and laboratory activities.

You will collaborate with lab, production, and quality teams, document precisely, and contribute to method development and investigations. This role offers hands-on technical growth and opportunities to lead improvements in a GMP environment.

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