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Job Description
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 key member of our Manufacturing Science and Technology (MS&T) department in Melbourne, Australia, the Engineer III will play a crucial role in enhancing our Drug Substance manufacturing capabilities. This role involves supporting the technology transfer of Moderna’s vaccine process, process validation, and life cycle CMC activities, establishing strong relationships across various departments.
Here’s What You’ll Do:
Within 3 Months, You Will…
Begin involvement in the technology transfer activities of commercial products to the new Australia site.
Start acting as a technical expert in cGMP manufacturing, including authoring technology transfer documents and supporting change controls.
Initiate analysis of manufacturing performance and start authoring manufacturing summary reports.
Within 6 Months, You Will…
Lead cross-functional troubleshooting and operational improvements for manufacturing processes and equipment.
Author and execute protocols supporting process characterization and equipment scale-up in cGMP Manufacturing.
Ensure continuous alignment with other global manufacturing sites through shared knowledge and data.
Within 12 Months, You Will…
Establish and maintain effective data repositories and communication channels for manufacturing data and issues.
Play a pivotal role in enhancing and optimizing the manufacturing process and equipment at the Australia site.
Demonstrate significant contributions to Moderna’s global manufacturing capabilities and strategies.
Here’s What You’ll Bring to the Table:
Biochemical engineer, Chemical engineer, or Biochemistry background. BS with more than 6 years of experience or MS with more than 3 years experience in a pharmaceutical or biotechnology company
Process development or operational experience in one or more of the following bioprocessing unit operations: Enzymatic reaction, chromatography, tangential flow filtration, buffer formulation, drug product formulation, and aseptic filling.
Experience in providing technical support to cGMP manufacturing organization
Experience in working with single use consumables, SS tanks and skids
Experience in supporting tech transfer, change control, investigation, and data analysis.
Outstanding communication skills (verbal and written)
Ability to manage projects in a fast-paced environment.
Ability to effectively collaborate in a dynamic, cross-functional matrix environment.
Ability to adapt to new and challenging technical opportunities.
