Senior Quality Associate

CSL Behring

Base: $94,000 - $111,000; bonus/equity: incentive ...
Gmp manufacturing experience
Deviation management and closure
Change control facilitation
The role ensures compliance with GMP/GSP/GxP by providing quality guidance across all phases of Technical Product Development

Job Summary

  • The role ensures compliance with GMP/GSP/GxP by providing quality guidance across all phases of Technical Product Development.
  • Responsibilities include managing complex deviations, facilitating Deviation Review Board meetings, and overseeing change controls to ensure regulatory adherence.
  • CSL Behring offers a culture of inclusion and belonging, driving innovation through a diverse workforce serving patients globally.

Matching Summary

The role ensures compliance with GMP/GSP/GxP by providing quality guidance across all phases of Technical Product Development.

Salary

Base: $94,000 - $111,000; Bonus/Equity: Incentive compensation and equity may be included; Benefits: Not specified

Skills & Requirements

Must-have

  • GMP manufacturing experience
  • Deviation management and closure
  • Change control facilitation
  • Product technical complaint handling
  • Self-inspection execution

Nice-to-have

  • Clinical trial GMP knowledge
  • Strong negotiation skills
  • Cross-functional communication
  • Continuous improvement mindset
  • Customer focus orientation

Key Requirements

  • Degree in biological science
  • 3 years experience in GMP or QA
  • Experience in pharmaceutical industry

Work Rights

Not specified

Tailored Resume

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