CSL Plasma is seeking a GMP Coordinator in Schwalmstadt, Germany, responsible for creating and managing GMP-related documents while ensuring compliance with regulatory requirements. The role emphasizes communication with quality assurance and involvement in deviation management
Job Summary
The role involves creating, maintaining, and archiving GMP-relevant documents for routine processes and global projects like PACE.
Candidates will monitor document conformity with European, American, and other regulatory standards while coordinating with the Quality Assurance department.
CSL Plasma operates one of the world's largest plasma collection networks, utilizing collected plasma to manufacture life-saving therapies in over 100 countries.
Matching Summary
Match Score: 80
CSL Plasma is seeking a GMP Coordinator in Schwalmstadt, Germany, responsible for creating and managing GMP-related documents while ensuring compliance with regulatory requirements. The role emphasizes communication with quality assurance and involvement in deviation management.
Skills & Requirements
Must-have
GMP relevant document creation and maintenance
English language proficiency Level 2
4-5 years of pharmaceutical industry experience
Knowledge of European and American regulatory requirements