Qualitätsmanagementbeauftragter (m/w/d) Für Unser Plasmacenter Göttingen

CSL Plasma

Göttingen, Germany
Quality management system oversight
Gmp document creation and approval
Audit preparation and execution
The role ensures the highest quality and safety standards for donors and patients through continuous process optimization

Job Summary

  • The role ensures the highest quality and safety standards for donors and patients through continuous process optimization.
  • Candidates will lead audits, manage deviations, and coordinate GMP documentation within a global biopharma environment.
  • CSL Plasma offers a mission-driven culture focused on patient care, innovation, and integrity with opportunities for professional growth.

Matching Summary

The role ensures the highest quality and safety standards for donors and patients through continuous process optimization.

Skills & Requirements

Must-have

  • Quality management system oversight
  • GMP document creation and approval
  • Audit preparation and execution
  • Process optimization and deviation handling
  • Staff training and quality awareness

Nice-to-have

  • Innovative problem-solving mindset
  • Strong team collaboration skills
  • Experience in plasma center operations
  • Leadership in quality improvement projects

Key Requirements

  • Degree in natural sciences, medicine, or pharmacy
  • Prior experience in pharmaceutical quality management
  • Advanced German and good English language skills
  • Proficiency with Office software and EDV tools

Work Rights

Not specified

Tailored Resume

Cover Letter