Teams at GSK

Lead investigations and CAPA, deliver process improvement and technical transfer projects, support validation and trials, monitor process trends, prepare technical documentation, and collaborate with manufacturing, quality, MSAT and maintenance to enable safe, compliant, and efficient vaccine and medicine production.

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.

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.