Qc Stability Associate

cslbehring.ch

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Stability study lifecycle support
Prepare routine protocols
Compile data
** CSL Behring is seeking a QC Stability Associate responsible for supporting stability studies, including data management and basic statistical analysis, within a GMP environment. The ideal candidate should possess at least an Associate degree in a science-related field and have 2+ years of experience in the pharmaceutical industry. **

Job Summary

  • The Stability Associate is responsible for executing day-to-day activities to support stability study lifecycle s.
  • This role requires a basic understanding of stability principles and has the ability to work well independently but under instruction and guidance of the line manager.
  • CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, 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 Behring is seeking a QC Stability Associate responsible for supporting stability studies, including data management and basic statistical analysis, within a GMP environment. The ideal candidate should possess at least an Associate degree in a science-related field and have 2+ years of experience in the pharmaceutical industry. **

Skills & Requirements

Must-have

  • stability study lifecycle support
  • prepare routine protocols
  • compile data
  • basic statistical analysis
  • GMP, ICH guidelines compliance
  • electronic systems for data management

Nice-to-have

  • initiative and accountability
  • readiness to develop knowledge
  • curiosity and empathy
  • celebrating differences

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter