Manufacturing Associate, Drug Substance - Shift Position

at  Moderna

• We are excited to announce that we are expanding our team and have multiple positions available for this role - join us in shaping the future!*

THE ROLE:

Joining Moderna offers the unique opportunity to be part of a pioneering team that’s revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you’ll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna’s commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients’ lives worldwide.
Moderna is committed to enhancing Australia’s biotech landscape through a long-term partnership that focuses on strengthening pandemic resilience. Our Melbourne-based large-scale mRNA vaccine manufacturing facility will be a cornerstone in Australia’s ability to respond to future health threats efficiently. This collaboration not only brings cutting-edge medical technology to the forefront but also emphasizes job creation and local talent development. We’re inviting visionary professionals to be part of this transformative journey, making a tangible impact on global health security.
As a Manufacturing Associate in the Drug Substance division at Moderna’s Resilience Site in Australia, you will play a crucial role in the production of mRNA vaccines. This position demands a blend of scientific knowledge, operational expertise, and digital proficiency. You’ll be an integral part of a team dedicated to producing safe and effective vaccines, upholding strict cGMP compliance and contributing to operational excellence in a dynamic, technology-driven environment.

HERE’S WHAT YOU’LL DO:

Within 3 Months, You Will…
Master safe work practices and adhere to Moderna’s safety procedures and guidelines.
Get accustomed to gowning procedures and maintain housekeeping standards in your assigned area.
Begin participating in incident investigations and CAPA tasks.
Within 6 Months, You Will…
Execute operational activities with adherence to cGMP, SOPs, and manufacturing documentation.
Collaborate closely with QA for documentation closure needed for commercial batch disposition.
Engage in troubleshooting routine equipment, process, and digital issues promptly.
Within 12 Months, You Will…
Actively participate in investigations of deviations and CAPA tasks.
Maintain training records and associated documentation.
Contribute to continuous improvement projects, demonstrating agility and adaptability in a fast-paced environment.