Jobs at GSK

Perform routine analytical and biochemical QC testing, review and approve test data for release, support investigations and CAPA, contribute to method/equipment validation, maintain lab documentation, coach colleagues, and support continuous improvement and data integrity in a regulated pharmaceutical laboratory.

Support set-up and operation of end-to-end biologics manufacturing (media prep, intermediates, drug substance). Ensure cGMP compliance, participate in commissioning/qualification, draft SOPs and documentation, lead and train staff, drive continuous improvement, and maintain safety and quality standards.

Lead site EHS and process safety for a major Singapore manufacturing project: manage risk, investigations, MOC, audits, compliance reporting, engineering reviews, training, and coach site teams to improve safety systems.

Lead and support site operational programs to ensure compliance with GSK quality and manufacturing systems for pharmaceuticals, OTC drugs, and medical devices. Support training, CAPAs, root cause analysis, non-conformance reports, audits, calibration verification, SOPs, and quality checks. Drive alignment with cGMP requirements and continuous improvement.

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.

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 Senior Manufacturing Engineer will deliver effective process engineering solutions, support technology transfer, lead site investigations, ensure compliance with standards, and collaborate to enhance manufacturing processes.

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.

Lead safe and efficient manufacturing operations, manage investigations, design process improvements, support technical transfers, and prepare technical 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.

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.

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

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

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

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

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.