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

Seqirus / CSL Plasma

Göttingen, Germany
Gmp document creation and approval
Statistical process control rule cards
Deviation and incident management
The role focuses on ensuring the highest quality and safety standards for donors and patients within the plasma center

Job Summary

  • The role focuses on ensuring the highest quality and safety standards for donors and patients within the plasma center.
  • Responsibilities include overseeing the Quality Management System, managing deviations, and approving GMP documents like SOPs.
  • The position offers the opportunity to lead quality improvement projects and collaborate with a global biopharma network.

Matching Summary

The role focuses on ensuring the highest quality and safety standards for donors and patients within the plasma center.

Skills & Requirements

Must-have

  • GMP document creation and approval
  • Statistical process control rule cards
  • Deviation and incident management
  • Audit preparation and execution
  • Employee training organization

Nice-to-have

  • Innovative quality solution development
  • Cross-functional team collaboration
  • Change coordination experience
  • Project leadership for expansion
  • Strong analytical problem-solving skills

Key Requirements

  • Degree in natural sciences, medicine, or pharmacy
  • Experience in pharmaceutical quality management
  • Advanced German and good English language skills
  • Proficiency with MS Office software

Work Rights

Not specified

Tailored Resume

Cover Letter