Qc Stability Associate

CSL Seqirus

Not specified
Basic understanding of stability principles
Experience in pharmaceutical manufacturing
Knowledge of gmp and ich guidelines
CSL Seqirus is seeking a QC Stability Associate to support the stability study lifecycle by preparing protocols, compiling data, and conducting basic statistical analyses. The ideal candidate should have a background in science, preferably with experience in the pharmaceutical industry, and a solid understanding of stability principles and compliance guidelines

Job Summary

  • The Stability Associate is responsible for executing day-to-day activities to support stability study lifecycles.
  • This role requires a basic understanding of stability principles and the ability to work independently under guidance.
  • CSL Seqirus is committed to inclusion and belonging, fostering a diverse workforce to connect with patients and stakeholders.

Matching Summary

Match Score: 75

CSL Seqirus is seeking a QC Stability Associate to support the stability study lifecycle by preparing protocols, compiling data, and conducting basic statistical analyses. The ideal candidate should have a background in science, preferably with experience in the pharmaceutical industry, and a solid understanding of stability principles and compliance guidelines.

Skills & Requirements

Must-have

  • Basic understanding of stability principles
  • Experience in pharmaceutical manufacturing
  • Knowledge of GMP and ICH guidelines

Nice-to-have

  • Collaboration and teamwork skills
  • Learning agility in scientific knowledge
  • Attention to detail

Key Requirements

  • Associate degree in science-related subject
  • 2+ years’ experience in stability program management
  • Fluency in English

Work Rights

Not specified

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