Jobs at GSK

Leads quality control activities for new vaccine projects, including analytical method development, validation, verification, transfer, equipment qualification, and testing. Coordinates with global QC and MSAT teams, ensures GMP and regulatory compliance, prepares validation plans and documentation, manages project budgets, and supports the transition from project to routine QC operations. Also drives knowledge transfer, training, laboratory quality systems, investigations, and continuous improvement.

Provides QA oversight across pharmaceutical manufacturing and QC operations to ensure cGMP compliance. Responsibilities include batch and equipment release authorization, documentation review, deviation and laboratory investigation management, CAPA and change-control oversight, audits, risk assessments, inspections, SOP ownership, training, and continuous quality improvement.

Leads Quality R&D operations for GMP pilot-plant manufacturing, storage, distribution, and validation. Ensures compliant production of cell banks, APIs, drug substances, and drug products under cGMP/cGDP. Oversees quality systems, governance, deviations, CAPA, change control, inspections, audits, risk management, technology transfers, and regulatory readiness. Builds organizational capability, leads change initiatives, manages EHS risks, and supports product launches and clinical supply requirements.

Leads Electrical and Automation Technicians at a regulated pharmaceutical manufacturing site. Oversees maintenance, troubleshooting, repair, commissioning, qualification, shutdowns, equipment handovers, contractor management, and capital project support for electrical, automation, instrumentation, and utility systems. Ensures compliance with EHS, cGMP, GEP, GDP, quality, and audit requirements. Coaches technicians, drives reliability and continuous improvement initiatives, manages CMMS records, and coordinates work with Operations, Engineering, Production, Utilities, suppliers, and contractors.

Support safe, compliant, and efficient on-site pharmaceutical manufacturing by leading deviation investigations, CAPA, process improvement projects, validation and technical transfers; monitor process trends, prepare technical documentation and training, and collaborate with manufacturing, quality, MSAT and maintenance to meet production goals.

Support safe, compliant manufacturing at the Singapore site by leading deviation investigations, CAPA, process improvement projects, validation and technical transfers, monitoring process trends, preparing technical documentation, and collaborating with manufacturing, quality, MSAT and maintenance teams.

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.

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.

Participate in a 15-month structured training programme focused on supply and production planning at a GMP-regulated vaccine manufacturing site. Learn supply continuity, scenario planning, reporting with Power BI, SAP operations, quality systems, and stakeholder management. The role requires attention to detail, problem-solving, communication, adaptability, teamwork, and a continuous improvement mindset. Applicants must hold a bachelor’s degree and be Singapore Citizens or Permanent Residents.

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.

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

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

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.

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.