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. In this lab‑based position reporting to the Associate Director of Quality Control, you will play a key role in performing cGMP QC testing to support Chemistry, Release, and Stability functions and support global GMP stability programs through a variety of operational and technical activities.
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. Our Melbourne‑based large‑scale mRNA vaccine manufacturing facility is a cornerstone in Australia's ability to respond to future health threats efficiently, emphasizing job creation and local talent development.
Here's What You'll Do
* Perform GMP QC Chemistry methods including HPLC, UPLC, UV, and Particle Analysis via Dynamic Light Scattering.
* Execute HPLC (AEX) and NaOH plate reader‑based assays to support process stat testing.
* Support method transfer projects internally and externally in collaboration with Analytical Sciences & Technology (AS&T) teams.
* Execute general lab operational tasks aligned with cGMP, including reagent preparation, equipment maintenance, and good documentation practices.
* Provide audit support for both internal and regulatory inspections.
* Create, review, and revise SOPs, protocols, and reports aligned with evolving quality standards and compliance frameworks.
Additional Responsibilities
* Support all stability program operations: perform sample set downs, pulls, inventory checks, labeling, and data entry in LIMS and inventory systems.
* Maintain and trend stability data using statistical analysis; produce stability tables, charts, protocols, and final reports.
* Troubleshoot assay methods and lab equipment as needed.
* Author or contribute to quality system documentation such as investigations, deviations, CAPAs, and change controls.
* Assist in the continued optimization of stability and QC workflows, ensuring seamless compliance and operational readiness.
Key Mindsets
* Obsess over learning: rapidly absorb new testing technologies, regulatory standards, and evolving data workflows.
* Digitize everywhere possible: embrace digital platforms like LIMS for sample tracking, inventory control, and data analysis.
What You'll Bring
* BSc in a relevant scientific discipline (Chemistry preferred) with 5 years Quality Control experience in a cGMP organization focusing on Analytical Chemistry.
* Hands‑on experience with analytical chemistry techniques including HPLC, UPLC, particle analysis, and plate reader‑based assays.
* Working knowledge of current FDA, EU, ICH guidelines and regulations.
* Experience working in a GMP environment.
* Ability to collaborate effectively in a dynamic, cross‑functional matrix environment.
* Ability to efficiently prioritize and complete multiple projects and tasks in a fast‑paced environment.
* Proven ability to conduct investigations.
* Site‑based; this position requires full‑time presence at Moderna's Melbourne site; it is not eligible for remote work.
* Potential to undergo pre‑employment and periodic medical assessments in line with relevant legal and operational requirements.
Pay & Benefits
* Best‑in‑class healthcare, plus voluntary benefit programs to support unique needs.
* Holistic well‑being: access to fitness, mindfulness, and mental health support.
* Family‑building benefits, including fertility, adoption, and surrogacy support.
* Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year‑end shutdown.
* Savings and investments to help you plan for the future.
* Location‑specific perks and extras.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world‑class team. By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. We believe in giving our people a platform to change medicine and an opportunity to change the world.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. We believe an in‑person culture is critical to our success, and we maintain a 70/30 in‑office work model to foster collaboration, innovation, and mentorship.
Moderna is a smoke‑free, alcohol‑free, and drug‑free work environment. We are committed to equal opportunity in employment and non‑discrimination for all employees and qualified applicants without regard to race, color, sex, gender identity or expression, age, religion, nationality, ancestry, disability, veteran status, or any other protected characteristic. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. All applicants requiring accommodations for the hiring process or to perform essential functions of the position can contact the Accommodations and Adjustments team at .
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