Qc Stability Associate

cslbehring.cl

Not specified
Basic understanding of stability principles
Experience in pharmaceutical manufacturing
Familiarity with electronic systems
CSL Behring is seeking a QC Stability Associate responsible for managing the stability study lifecycle, including data compilation and basic statistical analysis. The ideal candidate should have an associate degree or higher in a related science field and at least two years of experience in the pharmaceutical industry, particularly in stability program management

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 better with patients and stakeholders.

Matching Summary

Match Score: 75

CSL Behring is seeking a QC Stability Associate responsible for managing the stability study lifecycle, including data compilation and basic statistical analysis. The ideal candidate should have an associate degree or higher in a related science field and at least two years of experience in the pharmaceutical industry, particularly in stability program management.

Skills & Requirements

Must-have

  • Basic understanding of stability principles
  • Experience in pharmaceutical manufacturing
  • Familiarity with electronic systems

Nice-to-have

  • Collaboration and teamwork
  • 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

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