Manage a team for instrumentation engineering projects, ensure plant modifications and maintenance comply with standards, and supervise junior staff.

Assist with vaccine manufacturing processes through data analysis, documentation, and collaboration. Gain exposure to product lifecycle management and real-world data systems.

The role involves supervising and optimizing manufacturing processes, ensuring compliance with cGMP standards, and supporting quality investigations while documenting procedures and improvements.

As a Biotechnologist in the Career Conversion Programme, you will support the production of bulk drug substances, ensure compliance with safety and quality standards, and maintain production facilities.

Design, improve, and support manufacturing processes while collaborating with various teams, troubleshooting issues, and providing training and technical guidance.

The role involves designing and running experiments, analyzing data for process improvement, and supporting technology transfer to manufacturing. Requires hands-on lab experience and good documentation skills.

The role involves process engineering, equipment design standardization, collaboration on new technology evaluation, and documentation related to manufacturing and capital projects.

The internship involves supporting daily production activities, participating in commissioning processes, coordinating with stakeholders, driving improvement projects, and revising operational documents.

This role involves supervising changeover operations, ensuring compliance with cGMP, conducting safety investigations, and improving efficiency in biopharmaceutical manufacturing.

Six-month, full-time internship (Jan–Jun 2027) for current undergraduates enrolled at Singapore universities. Interns work on live projects across functions—commercial operations, data analytics, manufacturing, QA/QC, regulatory affairs, supply chain, marketing, sustainability—applying technical knowledge and developing interpersonal, communication and negotiation skills while experiencing GSK culture.

The trainee will ensure cGMP compliance in manufacturing, conduct quality checks, authorize documentation, and support quality investigations in the biopharmaceutical sector.

The role involves ensuring compliance with quality standards in biopharmaceutical manufacturing, providing QA consultation, managing KPIs, and implementing compliance initiatives.

This role involves providing technical and business analysis for MES applications, managing deployment, testing, validation, and improving manufacturing processes.

The role involves managing maintenance teams, overseeing plant modifications, ensuring GMP compliance, and supervising technicians to achieve operational targets in the biopharmaceutical industry.

Assist in process improvement, data analysis, project support, documentation, and collaboration with different departments in vaccine manufacturing.

Traineeship QA Operations role supporting cGMP compliance in vaccine manufacturing: perform QA checks, review and approve batch records and quality documentation, assist investigations, CAPA and change control, perform audits and risk assessments, and support product quality activities.

The role involves leading process investigations, driving improvements, and supporting equipment validation and technical transfers while ensuring compliance with safety and quality standards.

Support Manufacturing Operations by managing deviation investigations, optimizing processes, and participating in technology transfers while ensuring compliance with regulations.

The internship involves supporting operational excellence activities, continuous improvement using Lean Six-Sigma, driving projects, and developing solutions for Smart Manufacturing.