Qc Stability Associate

CSL Behring

Liverpool, United Kingdom
Basic understanding of stability principles
Experience in pharmaceutical manufacturing
Knowledge of gmp and ich guidelines
The Stability Associate is responsible for executing day-to-day activities to support stability study lifecycles

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 values inclusion and belonging, fostering a diverse workforce that drives innovation.

Matching Summary

The Stability Associate is responsible for executing day-to-day activities to support stability study lifecycles.

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
  • 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

Tailored Resume

Cover Letter