Quality Assurance For Quality Control, Australia

Moderna

Clayton, Australia
**
Cgmp regulations compliance
Alcoa+ data integrity
Analytical method lifecycle management
** Moderna is seeking a Quality Assurance professional for its Quality Control function in Clayton, Australia, to ensure compliance with global cGMP regulations and support end-to-end laboratory operations. The role offers the opportunity to contribute to a pioneering mRNA technology team while engaging in rigorous quality oversight and inspection readiness. **

Job Summary

  • This high-impact individual contributor role provides Quality Assurance (QA) oversight to the Quality Control (QC) function at Moderna’s Melbourne-based Resilience site.
  • You’ll support end-to-end laboratory operations, align QC practices with global Moderna sites, and ensure 24/7 inspection readiness across the QC function.
  • Moderna offers best-in-class healthcare, a holistic approach to well-being, family building benefits, and generous paid time off.

Matching Summary

Match Score: 75

** Moderna is seeking a Quality Assurance professional for its Quality Control function in Clayton, Australia, to ensure compliance with global cGMP regulations and support end-to-end laboratory operations. The role offers the opportunity to contribute to a pioneering mRNA technology team while engaging in rigorous quality oversight and inspection readiness. **

Skills & Requirements

Must-have

  • cGMP regulations compliance
  • ALCOA+ data integrity
  • analytical method lifecycle management
  • microbiology operations oversight
  • OOS/OOT investigation management
  • risk-based assessments ICH Q9

Nice-to-have

  • global QC ecosystem collaboration
  • generative AI tools in QC
  • proactive risk identification
  • continuous improvement initiatives

Key Requirements

  • Bachelor’s Degree in a scientific field
  • 7 years of Biopharmaceutical / Pharmaceutical Industry experience
  • Strong working knowledge of cGMP regulations
  • Experience with regulatory inspections as SME
  • Demonstrated experience in method validation
  • Experience with OOS/OOT investigation management

Work Rights

Not specified

Tailored Resume

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