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You will lead Manufacturing Sciences and Technology (MSAT) product owner activities in Singapore. You will work closely with manufacturing, quality, engineering and technical transfer teams to ensure safe, compliant and efficient product operations. You will resolve technical issues, lead process improvements, and drive site product lifecycle management. We value curious problem-solvers who communicate clearly, act with integrity, and enjoy working in collaborative teams. This role offers growth through technical leadership, cross-functional exposure and the chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together.
Job Responsibility
Lead technical stewardship for assigned products during scale-up, commercial manufacture, and continuous improvement
Investigate and resolve product and process issues, using root cause analysis and evidence-based recommendations
Support technical transfers and start-ups by creating transfer packages, validating processes, and coaching receiving teams
Partner with manufacturing, quality and regulatory colleagues to ensure compliance and to prepare technical documentation for change controls and deviations
Drive process reliability and efficiency projects using data, risk assessments, and robust controls
Mentor junior engineers and share knowledge across sites and teams
Requirements
Bachelor’s degree in chemical engineering, biochemical engineering, pharmaceutical sciences or related field
Minimum 8 years’ experience in pharmaceutical biologics manufacturing, process development or MSAT
Practical experience with technology transfer, process troubleshooting and deviation investigations
Strong knowledge of GMP principles and experience working with quality systems
Demonstrated ability to analyze data, lead root cause analysis and implement corrective actions
Effective communicator with experience working in cross-functional teams and managing stakeholders
Nice to have
Advanced degree (master’s or PhD) in a relevant discipline
Experience with aseptic processing or vaccine manufacturing
Familiarity with process validation, statistical tools and continuous improvement methods
Hands-on experience in a multi-site or global network environment
Experience preparing technical reports for regulatory submission
Prior program leadership experience (matrix leadership)