QC Job at GSK, Singapore | Life Sciences | Apply Now
If you are an analytical chemist, biochemist, or laboratory analyst looking to accelerate your career within a world-class manufacturing network, this full-time role at GSK is an exceptional opportunity. Located at GSK’s cutting-edge biopharmaceutical hub in Tuas, Singapore, this position places you on the front lines of data integrity, quality control, and compliance execution. For technical specialists searching for a high-impact QC Job, this position offers hands-on mastery over routine and non-routine analytical testing, Out-of-Specification (OOS) investigations, and automated LIMS architectures. It serves as an elite launchpad for a long-term GSK career and stands out as a premier choice for anyone tracking a competitive Biotechnology Job within Singapore’s booming global biomedical corridor.
- Job Position: QC Associate
- Location: Tuas, Singapore
- Category: Quality
- Job ID: 443495
About The Company
GSK is a leading global biopharma company driven by a singular purpose: to unite science, technology, and talent to get ahead of disease together. Aiming to positively impact the health of 2.5 billion people by the end of the decade, GSK focuses on developing innovative specialty medicines and vaccines across four therapeutic areas: infectious diseases, HIV, oncology, and respiratory/immunology. The state-of-the-art manufacturing campus in Tuas, Singapore, functions as a highly automated, high-compliance production asset within GSK’s global network. Joining the Tuas Quality Control team as a Direct Staff member means operating in an environment built on strict GxP regulations. Here, raw ingredients, active pharmaceutical ingredients (APIs), and finalized vaccines are systematically verified before global distribution.
QC Job – Key Responsibilities
The QC Associate assumes daily operational ownership over sample lifecycles, data validation, and laboratory troubleshooting to ensure materials meet strict compendial and regulatory benchmarks.
Your core testing, compliance, and investigation duties will include:
- Analytical Testing Execution: Performing routine and non-routine analytical chemistry testing, biochemical assays, or microbial plates using validated methodologies and specialized instrumentation.
- Sample Chain of Custody: Managing the end-to-end sample lifecycle, including receipt, triage, safe storage, and final disposition to guarantee absolute traceability.
- OOS & Atypical Investigations: Leading or supporting thorough investigations into Out-of-Specification (OOS) or atypical laboratory results to identify root causes and drive Corrective and Preventive Actions (CAPA).
- Equipment Calibration & Care: Maintaining, calibrating, and troubleshooting analytical laboratory equipment, ensuring all instruments remain in a qualified state.
- Data Integrity & Review: Recording and auditing raw experimental data sets under strict Good Documentation Practices (GDP), utilizing basic data analysis in Excel for quality trending.
- Method Transfers & Validation: Contributing to localized method transfers, validation/verification activities, and site-level continuous improvement projects using lean management frameworks.
Qualifications & Profile Requirements For QC Job
GSK seeks an organized, detail-oriented life scientist who possesses the collaborative agility to work efficiently under routine shift patterns when required.
- Required Academic & Experience Criteria:
- Educational Foundation: A formal Diploma or Bachelor’s degree in Biology, Biochemistry, Biotechnology, or a related life science field.
- Industry Track Record: A minimum of 2 years of practical laboratory experience operating within a regulated analytical environment.
- Regulatory Grounding: Strong functional knowledge of Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and general GxP regulations.
- Linguistic Mastery: Clear written and spoken English language skills, paired with highly accurate technical documentation habits.
- Preferred Assets & Leadership Capabilities:
- Practical experience handling biological testing, microbiology techniques, or specific biochemical assays.
- Familiarity navigating electronic data management tools, digital tracking applications, or Laboratory Information Management Systems (LIMS).
- Prior experience participating in equipment qualifications, instrument validations, or lean lab initiatives.
- Strong problem-solving, communication, and peer coaching skills (as a senior associate, you will actively guide junior analysts and help lead investigation workflows).
In short, the QC Associate position at GSK is a definitive route to transitioning your chemistry or biotechnology degree into a highly valuable biomanufacturing asset. Securing this appointment allows you to move past basic classroom lab exercises and take direct operational charge of the OOS investigations, analytical assays, and automated LIMS data flows that protect global patient safety. If you reside in Singapore, meet the 2-year analytical threshold, and possess an compromise-free commitment to data integrity, apply today to secure this premier QC Job, launch a highly rewarding GSK career, and lock in this outstanding Biotechnology Job.
