Location: Woolloongabba, Brisbane QLD

This role reports directly to the Head of Vaccine Project Management and is responsible for the setup, delivery and review of the vaccine development projects. The Project Manager ensures project timelines are met while maintaining compliance with quality and regulatory standards.

Location: Woolloongabba, Brisbane QLD

Reporting to the Head of Quality this role will take responsibility for the leadership of part of the Quality team and drive the ongoing implementation of the Quality Management System to deliver improvements across all relevant areas of the business.

Location: Woolloongabba, Brisbane QLD

The Medical Device Engineer role provides operational, manufacture and maintenance support to Vaxxas' in-house laser facilities for the micro-machining of medical device components for R&D and clinical activities. The role will require the candidate to operate and maintain laser systems and their accompanying services, work with various teams across the company to design and develop specialised tooling and micro-machining processes.

Location: Woolloongabba, Brisbane QLD

The Clinical Trial Assistant will be responsible for supporting the Clinical Trial Manager in the management of multiple clinical studies from study start-up activities to study close-out. Also responsible for performing on-site and remote site visits and supporting the Study Team in successful completion of multiple clinical studies in accordance with Vaxxas timelines.

Location: Woolloongabba, Brisbane QLD

Reporting to the Laboratory Manager, these positions will play a key role in maintaining the laboratory facilities and supporting our analytical scientists.

Location: Woolloongabba, Brisbane QLD

We are currently seeking a number of scientists for multiple new roles across disciplined areas to join our Formulation & Analytical and Preclinical teams as we expand in our scientific research & development.

These scientist roles will be responsible for supporting their respective teams to complete key processes or aspects of a broader project that support the successful completion of projects.

Location: Work from home / Work remotely

Reporting to the Head of Clinical and Regulatory Affairs this position is for a Senior Regulatory Affairs Associate within the Clinical and Regulatory team who is responsible for the preparation, management, and submission of regulatory applications to global health authorities. They are also responsible for liaising with external collaborators and providing regulatory guidance for all functional teams.