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The Senior Product Manager will oversee Clinical Safety and Pharmacovigilance Systems, ensuring system reliability and compliance while driving innovation and product strategy.

Senior QA role providing QC oversight at Moderna's Melbourne manufacturing site. Ensure cGMP and pharmacopoeial compliance across QC labs, manage method validation/transfers, lead OOS/OOT and deviation investigations, drive inspection readiness, oversee external labs, and support data integrity, risk-based decisions, and continuous improvement across global QC sites.

The Director of Process Development will lead upstream process development for E. coli-based production of enzymes and plasmids, setting technical strategy, leading execution, optimizing fermentation processes, and managing technology transfers.

The Senior Product Manager for Clinical Biomarker Systems will lead the strategy and management of digital platforms supporting clinical biomarker labs, ensuring compliance with regulations and quality standards, while driving product development and cross-functional collaboration.

The CMC Digital Support Lead oversees digital application support for CMC systems, ensuring compliance and improving service delivery through operational leadership and technical support for Lab and Quality systems.

Lead enterprise FP&A activities including consolidated budgeting, forecasting, long-range planning, and performance analysis. Partner with commercial, R&D, CMC, and G&A leaders to deliver management reporting, dashboards, and executive presentations, support month-end close, labor/benefits forecasting, scenario modeling, and process/tool improvements to enhance accuracy and scalability.

Support technology transfer and GMP manufacturing processes, ensuring technical oversight, data management, and compliance in collaboration with CMOs.

The Associate Director will lead stability strategies for mRNA products, ensuring compliance with regulatory standards and collaborating cross-functionally to enhance product development and supply chain operations.

As a Stability Leader, you'll define and execute stability strategies for mRNA programs, ensuring regulatory compliance and product quality through data analysis and cross-functional collaboration.

The Director, Technical Development Operations will build and lead a multidisciplinary team for bioassay operations, oversee critical assay execution, and implement GxP-compliant infrastructure while driving automation and integration with digital tools.