Jobs at GSK

Provide process and technical support to manufacturing operations in Singapore: lead investigations and CAPA, deliver process improvements, support validation/commissioning and technical transfers, maintain documentation and training, troubleshoot equipment and process issues, and manage change impact with cross-functional teams to ensure safe, compliant, and efficient production.

Support QA Operations by reconciling quality processes, scanning and archiving batch records, performing QA gemba walks, maintaining QA trackers, driving quality improvement (Kaizen) projects, and developing training guides and induction improvements for QA staff.

Lead setup and operation of end-to-end biologics manufacturing processes, ensuring cGMP compliance, quality, safety and project timelines. Support commissioning, SOP/OJT development, training and technology transfer, drive continuous improvement, assist deviation/CAPA investigations, and coordinate with QA/QC/Engineering to maintain robust production documentation and operational readiness.

Work on HBV product and process transfer projects supporting design, construction, testing and commissioning of vaccine manufacturing facilities. Assist work package managers, develop training matrices and change control documentation, and manage project documentation to meet milestones and ensure timely handover.

Assist in managing Quality Control projects, providing testing support to meet regulatory standards, and performing data extraction and analysis. Engage with various teams within GSK Vaccines.

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.

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

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

Provide QA oversight to ensure cGMP compliance across manufacturing and QC operations. Manage deviations, CAPA, change controls, authorizations, documentation review, investigations, risk assessments, audits, training, and continuous quality improvements to support batch release and regulatory compliance.

Perform and lead routine and non-routine analytical testing, manage sample lifecycle and chain of custody, investigate OOS results and support CAPA, maintain and troubleshoot lab equipment, record and review data per GLP/GxP, contribute to method transfers, validations and continuous improvement.

Assist in planning and logistics internships focused on productivity, data automation, performance management, and improving warehouse operations through innovative processes and tools.

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

This internship focuses on productivity improvement initiatives, involving automation, cycle time enhancement, yield optimization, and support for GSK's production system.

As a manufacturing intern, you'll assist engineers in optimizing manufacturing processes, troubleshoot issues, and learn about production of Active Pharmaceutical Ingredients, while gaining hands-on experience and skills in data analytics and documentation practices.

The internship involves collaborating with cross-functional teams, supporting process validation, collecting and analyzing data, and drafting technical documentation in vaccine manufacturing.

Internship focused on operational excellence and smart manufacturing. Tasks include supporting lean projects, automating processes, and fostering team collaboration in biopharma.

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

This internship involves supporting digitalization and automation in biopharma manufacturing, collaborating on electronic batch records, and improving workflows. Interns will gain practical exposure and learn about GMP practices, digital transformation, and system testing.

Assist in improving manufacturing processes through data analysis, Lean Manufacturing principles, project support, and documentation. Collaborate with cross-functional teams and participate in training sessions.

The internship involves supporting production engineering by monitoring equipment, troubleshooting, participating in investigations, and ensuring compliance with manufacturing practices.