Qualitätsmanagementbeauftragte

CSL Plasma

Bremen, Germany
Fully onsite
Gmp document creation and approval
Statistical process control rule cards
Audit preparation and execution
CSL Plasma is seeking a Qualitätsmanagementbeauftragte in Bremen, Germany, to ensure the highest quality standards in their plasma donation centers. The role involves overseeing quality management systems, process optimization, and team training, emphasizing a commitment to patient focus and innovation

Job Summary

  • The role involves ensuring the highest quality standards are met in plasma centers through continuous oversight and process optimization.
  • Candidates will be responsible for managing deviations, approving GMP documents like SOPs and risk analyses, and leading audit preparations.
  • CSL Plasma offers a mission-driven environment where quality and patient safety are central to saving lives globally.

Matching Summary

Match Score: 85

CSL Plasma is seeking a Qualitätsmanagementbeauftragte in Bremen, Germany, to ensure the highest quality standards in their plasma donation centers. The role involves overseeing quality management systems, process optimization, and team training, emphasizing a commitment to patient focus and innovation.

Skills & Requirements

Must-have

  • GMP document creation and approval
  • Statistical process control rule cards
  • Audit preparation and execution
  • Deviation and incident management
  • SOP and WI development

Nice-to-have

  • Change coordination experience
  • Project leadership for quality improvement
  • Team training and development skills
  • Innovative problem-solving mindset
  • Cross-functional collaboration abilities

Key Requirements

  • Degree in natural sciences, medicine, or pharmacy
  • Prior experience in pharmaceutical quality management
  • Advanced German and good English language skills

Work Rights

Not specified

Tailored Resume

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