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

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

As a Biotechnologist Intern, you will assist in vaccine production, learn Good Manufacturing Practices, perform key computer applications, and support preventive maintenance activities.

Lead engineering activities for equipment maintenance and capital projects, ensuring compliance and mentoring junior staff in a regulated environment.

The QC Specialist will perform quality control testing in laboratories, review test data, support investigations, and contribute to method validation while coaching colleagues.

Lead sterility assurance and microbiology quality activities for site manufacturing, including SOPs, validations, investigations (OOS/OOT), environmental monitoring, audits, CAPA, and cross-functional support for product release and change control.

Lead QA activities and ensure compliance with cGMP during product transitions. Author quality plans and oversee manufacturing processes, deviations, and audits.

Lead quality assurance activities by providing oversight for validation projects, drafting validation documents, and assessing impact on validation status. Collaborate with teams, ensuring compliance with regulatory standards while fostering communication across functions.

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.

Manage production activities for bulk drug substances ensuring compliance with quality and safety regulations, while leading and developing a team.

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

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

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

Lead quality activities for small molecule R&D, ensuring compliance with GMP and regulatory standards, managing audits, documentation, and risks, while fostering a culture of continuous improvement.

As Site Procurement Specialist, you will drive procurement initiatives, manage supplier relationships, ensure compliance, and identify process improvements across multiple categories.

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

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

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

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

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.