Qc Stability Associate

CSL Seqirus

Not specified
Stability study lifecycle support
Prepare routine stability protocols
Compile and update data tables
CSL Seqirus is seeking a QC Stability Associate to support the stability study lifecycle, requiring a basic understanding of stability principles and the ability to work independently under guidance. The ideal candidate should have 2+ years of experience in the pharmaceutical industry and familiarity with GMP and ICH guidelines

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, 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, requiring a basic understanding of stability principles and the ability to work independently under guidance. The ideal candidate should have 2+ years of experience in the pharmaceutical industry and familiarity with GMP and ICH guidelines.

Skills & Requirements

Must-have

  • Stability study lifecycle support
  • Prepare routine stability protocols
  • Compile and update data tables
  • Basic statistical analysis
  • GMP and ICH guidelines compliance
  • LIMS and JMP familiarity

Nice-to-have

  • Recognize unexpected results
  • Risk-based assessments awareness
  • Initiative and accountability
  • Learning agility
  • Collaboration and teamwork

Key Requirements

  • Associate degree in science related subject
  • 2+ years pharmaceutical manufacturing experience
  • Stability program development and management experience
  • Fluency in English

Work Rights

Not specified

Tailored Resume

Cover Letter