Qc Stability Associate

CSL Seqirus

Not specified (suggested: hybrid)
Stability study lifecycle support
Prepare routine protocols
Compile data
CSL Seqirus is seeking a Qc Stability Associate to support the stability study lifecycle, focusing on data management, statistical analysis, and compliance with GMP and ICH guidelines. The role requires a basic understanding of stability principles, strong attention to detail, and the ability to work collaboratively within a team

Job Summary

  • The Stability Associate is responsible for executing day-to-day activities to support stability study lifecycle s.
  • Main Responsibilities include supporting stability programs, providing knowledge and understanding of stability principles, and working collaboratively with QC Operations.
  • CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness.

Matching Summary

Match Score: 75

CSL Seqirus is seeking a Qc Stability Associate to support the stability study lifecycle, focusing on data management, statistical analysis, and compliance with GMP and ICH guidelines. The role requires a basic understanding of stability principles, strong attention to detail, and the ability to work collaboratively within a team.

Skills & Requirements

Must-have

  • stability study lifecycle support
  • prepare routine protocols
  • compile data
  • basic statistical analysis
  • GMP compliance
  • ICH guidelines

Nice-to-have

  • initiative and accountability
  • learning agility
  • collaboration and teamwork
  • problem recognition

Key Requirements

  • Associate degree (Level 5 vocational qualification)
  • 2+ years experience in pharmaceutical manufacturing
  • Fluency in English

Work Rights

Not specified

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