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

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

Assist in engineering support for the new HBV vaccine facility, including qualification activities, documentation, and project responsibilities while gaining hands-on experience in biopharmaceutical manufacturing.

The intern will support manufacturing engineers by optimizing production processes and improving product yield while gaining hands-on experience in troubleshooting, lean tools, and data analysis.

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

The intern will assist the QA GMP team, support day-to-day activities, manage records and trackers, and develop training materials.

You will support the GSK Production System team by collecting data, driving improvement projects, and assisting in workshops to enhance continuous improvement culture.

Assist in improving manufacturing processes through data analysis, implementing Lean principles, collaborating with departments, and supporting various project initiatives.

Intern will assist in managing Quality Control projects, support data extraction and analysis, and collaborate with varying teams for compliance with regulatory standards.

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

Provide on-site quality oversight for production and lab activities, review batch records and data integrity, lead investigations and corrective actions, approve QA operational tasks, perform internal audits and supplier assessments, and coach colleagues to maintain GMP compliance and inspection readiness.

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.

Lead the Singapore site engineering function to deliver safe, compliant, and reliable manufacturing operations. Shape engineering strategy, manage maintenance, projects and asset lifecycle, drive reliability and continuous improvement, and coordinate stakeholders across operations, quality, EHS, finance and suppliers.

Lead process and technical support for manufacturing value streams to meet operational and cGMP compliance goals. Manage deviation investigations and CAPAs, support validation and technical transfers, track process parameters, perform gap analyses, develop training and documentation, and drive continuous improvement and operational excellence projects to ensure reliable production delivery.

Provide process and technical support to manufacturing operations to meet production and cGMP compliance. Manage deviation investigations and CAPAs, support validation, process optimization, change control, gap analyses of quality systems, develop training and documentation, and lead continuous improvement and project execution within the value stream.

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

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

Support set-up and operation of end-to-end biologics manufacturing: media/buffer prep, intermediate and drug substance production, cGMP compliance, commissioning/qualification, documentation, training, continuous improvement, and cross‑department coordination. Senior biotechnologists provide leadership, training, and process subject-matter expertise.

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

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