Senior Quality Associate

CSL Behring

Base: $94,000 - $111,000; bonus/equity: incentive ...
Gmp manufacturing experience
Deviation investigation management
Capa and change control execution
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.
  • Candidates will manage complex deviations, facilitate Deviation Review Board meetings, and oversee the closure of significant quality issues.
  • CSL Behring is a global biotherapeutics leader employing 32,000 people who deliver therapies to over 100 countries.

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 investigation management
  • CAPA and change control execution
  • Technical complaint handling
  • Self-inspection facilitation

Nice-to-have

  • Clinical trial GMP knowledge
  • Product development environment experience
  • Strong negotiation skills
  • Cross-functional communication abilities
  • Continuous improvement mindset

Key Requirements

  • Degree in biological science
  • At least 3 years experience in GMP manufacturing, Regulatory Affairs, or Quality Assurance
  • Previous Production, Quality, or R&D experience in Pharmaceutical industry

Work Rights

Not specified

Tailored Resume

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