Teams 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.