Analyst, Quality Control, Chemistry & Stability (Melbourne)

The Role Overview Moderna invites you to join a pioneering team that is revolutionizing medicine through mRNA technology. In this lab-based position located at our Melbourne Resilience site, you will work under the Associate Director of Quality Control to perform cGMP QC testing and support Chemistry, Release, and Stability functions. As a QC Analyst, you will support global GMP stability programs through sample set-downs, pulls, shipments, data trending and statistical analysis. You will work in full compliance with cGMP standards, FDA, EU and ICH regulations while contributing to method transfers and ongoing qualification projects. This is an individual‑contributor position focused on operational execution and scientific rigor. Your Key Responsibilities
- Perform GMP QC Chemistry methods including HPLC, UPLC, UV, and particle analysis by Dynamic Light Scattering
- Execute HPLC (AEX) and NaOH plate-reader assays to support process stat testing
- Support method transfer projects internally and externally in collaboration with Analytical Sciences & Technology teams
- Carry out 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 in line with evolving quality standards 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 laboratory 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 Required Qualifications & Skills
- BSc in a relevant scientific discipline (Chemistry preferred) with at least 5 years of quality control experience in a cGMP organization focused on analytical chemistry
- Hands‑on experience with analytical chemistry techniques including HPLC, UPLC, particle analysis and plate‑reader assays
- Working knowledge of the relevant and 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 prioritize and complete multiple projects and tasks in a quick‑paced environment
- Proven ability to conduct investigations
- Site‑based; full‑time at the Melbourne site; remote work not eligible
- May be subject to pre‑employment and periodic medical assessments in line with local requirements Pay & Benefits
- Best‑in‑class healthcare, plus voluntary benefit programs to support unique needs
- Holistic well‑being access including fitness, mindfulness and mental health support
- Family‑building benefits (fertility, adoption, surrogacy support)
- Generous paid time off: vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year‑end shutdown
- Savings and investments to aid future planning
- Location‑specific perks and extras Equal Opportunity & Reasonable Accommodation Moderna is committed to equal opportunity in employment and non‑discrimination for all employees and qualified applicants regardless of personal characteristics protected under applicable law. We consider qualified applicants even with criminal histories consistent with legal requirements. All qualified applicants with disabilities will receive reasonable accommodation or adjustments during the hiring process and in the performance of job duties. #J-18808-Ljbffr Apply on Kit Job: kitjobau.com/job/3rwa2p