The Automation Engineer supports drug product manufacturing by troubleshooting PLC/SCADA systems, maintaining automation equipment, and ensuring GMP compliance through root cause analysis and process optimization activities.

The Production Engineer ensures the operability and compliance of mRNA drug manufacturing equipment, troubleshooting issues, supporting operations, and improving reliability in a GMP environment.

The Country Head, Regulatory Affairs will lead regulatory strategy for Australia and New Zealand, manage local regulatory compliance, and drive strategic partnerships to support local vaccine manufacturing.