Jobs at GSK

Perform analytical testing and sample management for intermediates/products, support method development/validation/transfer, operate and troubleshoot lab equipment, lead/support process improvements and projects, maintain documentation and compliance to GMP/GLP standards, and ensure inspection readiness.

Lead redesign of the global marketing agency ecosystem, defining a tiered agency model and AI-enabled content supply chain. Drive new ways of working, commercial and procurement models, governance, KPI frameworks, and strategic agency partnerships. Align transformation with end-to-end marketing operations, oversee change management, capability building, and continuous evolution of agency, in-house, and AI-enabled capabilities.

Lead design and delivery of a global content hub: define operating model, vendor strategy, transition plans, capability roadmap (modular content, AI-assisted production), integrate workflows and MarTech, drive adoption, and measure performance to improve speed, quality and cost across markets.

Lead the marketing technology roadmap and business case for end-to-end marketing transformation. Define target-state capabilities across people, process, and platforms; partner with Digital & Technology for architecture, integration, data foundations, measurement frameworks, and KPIs. Align enterprise marketing capability across Commercial and Medical, manage vendor/partner relationships, and ensure governance, compliance, and risk management to deliver scalable, AI-enabled marketing solutions.

Lead engineering and maintenance for production equipment in a cGMP pharmaceutical site. Manage equipment lifecycle from design review and commissioning through qualification, validation, preventive and corrective maintenance. Drive reliability, continuous improvement, CAPA, deviation investigations, CAPEX projects, budgeting, and contractor management to ensure safe, compliant, and efficient manufacturing operations.

Serve as site microbiology SME to develop monitoring strategies and frameworks; ensure cGMP-compliant analysis of water, environmental, utilities and product testing; perform microbiological risk assessments; manage external labs; lead/support audits and investigations; support R&D transfers and new product introductions; ensure regulatory compliance and implement remedial actions.

Join GSK's Production Engineering team to support biopharmaceutical manufacturing through hands-on training, ensuring equipment reliability and compliance, with opportunities for continuous improvement.

Work on Value Stream 2 enabling projects to support new product introductions. Lead operational improvement initiatives using Lean Six Sigma and data analytics (Power BI, Mtell, Power Apps, Excel), learn GMP and documentation practices, support qualification/HAZOP/FMEA activities, assist engineers with troubleshooting, and help manage consumables for manufacturing campaigns.

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

Six-month internship supporting QC lab productivity: map processes, identify waste, apply Lean/Kanban tools, pilot/configure an online tracking/scheduling application, promote green procurement, and support lab projects to deliver productivity gains and a working prototype with user guide.

Support engineers, chemists and data scientists to deploy smart manufacturing projects by collecting, extracting, analyzing, validating and visualizing process and business data. Build dashboards and low-code connected worker apps (MS Power Platform/BI), support operational excellence and change management, and assist with project communications and stakeholder engagement.

Support data scientists to structure and manage operational manufacturing data, build predictive ML models, develop dashboards/visualizations (Power BI/MS Power Platform), and assist project management and stakeholder communications during a January–June 2027 internship.

Support rollout of 5S and laboratory zoning, develop standard work and visual controls, update lab safety policies and SOPs aligned to Site Laboratory Excellence, deliver training, and support lab projects to achieve inspection readiness and improve GPS maturity.

Support Quality Operations by learning GMP principles, assessing manufacturing risks, proposing mitigations, and optimizing batch release processes to reduce lead time for APIs. Participate in plant GEMBAs, contribute to quality oversight, and work on project-based assignments to improve operational quality and process standardization.

Support engineers in GMP manufacturing activities: update SOPs, manage deviations and CAPAs, investigate process/equipment issues, assist equipment qualification, compile performance data, participate in continuous improvement and workflow mapping, and frequently work in cleanrooms.

Provide engineering support for a new HBV vaccine facility including utilities and equipment design review, acceptance testing, qualification, commissioning, documentation (P&ID, SOPs, work instructions), asset care and reliability activities, SAP master data and maintenance/calibration planning, and coordination with local/global engineering teams, contractors, quality and production.

Work with the GSK Production System team to support continuous improvement projects using Gemba, data collection and analysis (Excel), drive 5S and standard work, assist KPI dashboard improvements, coordinate site-wide GPS workshops and culture-improvement activities, and support GPS experts in fostering a continuous improvement culture.

Lead site process safety and EHS for a Singapore manufacturing site: manage risk, investigations, management of change, audits, compliance reporting, coaching, and support safe engineering changes and commissioning.

Support engineering activities for a new HBV vaccine facility including utilities and equipment qualification, design review, acceptance testing, qualification and commissioning. Assist with documentation review and drafting (P+ID, SOPs, risk assessments), asset care and maintenance programs, SAP master data and creation of maintenance/calibration plans, and collaborate with local and global engineering, quality, production teams and external vendors.

Lead and maintain site Quality Systems (Deviation, CAPA, Change Control, PQR, QMS) to ensure cGMP compliance and inspection readiness. Act as site SME, drive investigations, CAPA effectiveness, change control, quality alerts, risk management, audits/inspections, regulatory conformance, and continuous improvement. Coordinate governance, present metrics to Site Quality Council, support SAP/eQMS users, and manage QRM and EHS compliance.