Gmp-koordinator 3

CSL SEQIRUS

Schwalmstadt, Germany
Gmp-relevant document management
Sop creation and maintenance
Regulatory compliance monitoring
The role involves the creation, maintenance, and archiving of GMP-relevant documents such as SOPs, test instructions, and specifications

Job Summary

  • The role involves the creation, maintenance, and archiving of GMP-relevant documents such as SOPs, test instructions, and specifications.
  • Responsibilities include monitoring documents for GMP compliance, initiating corrective actions, and coordinating information between departments and global quality units.
  • CSL Plasma operates a large plasma collection network and uses collected plasma to manufacture life-saving therapies for patients worldwide.

Matching Summary

The role involves the creation, maintenance, and archiving of GMP-relevant documents such as SOPs, test instructions, and specifications.

Skills & Requirements

Must-have

  • GMP-relevant document management
  • SOP creation and maintenance
  • Regulatory compliance monitoring
  • Cross-functional information coordination
  • English language communication

Nice-to-have

  • Proactive problem identification
  • Collaborative team environment
  • Commitment to patient well-being

Key Requirements

  • 3.5-year vocational training
  • English Level 2
  • GMP specialization
  • 4-5 years of professional experience

Work Rights

Not specified

Tailored Resume

Cover Letter