About This Role
A QC Specialist role at GSK in Tuas, Singapore, requires a Bachelor's degree or Diploma with 2+ years of laboratory experience in regulated environments (pharma/biopharma), including analytical techniques, method validation, and CAPA implementation.
Responsibilities
- Perform routine analytical testing of raw materials and finished products using approved methods.
- Review test data for accuracy, compliance with regulations, and timely release decisions.
- Support investigations for deviations, out-of-specifications, and environmental incidents with corrective actions.
- Contribute to method validation, revalidation, and qualification activities including documentation.
- Coach colleagues on methods, instrumentation, data integrity, and standard operating procedures (Tiers, Gemba, DMAIC).
Requirements
- Bachelor's degree in Life Science, Chemistry, Biochemistry, Microbiology or related field.
- Minimum 2 years of laboratory experience in a regulated environment (preferably pharmaceutical or biopharma).
- Practical experience with analytical techniques or biochemistry methods relevant to quality control.
- Knowledge of Good Manufacturing Practice and laboratory quality systems.
- Strong record keeping, report writing, and basic investigation skills.
- Capability in problem-solving to identify, report, resolve, and escalate issues promptly.