Quality Manager (all genders) Batch Record Review – Biotechnological Products

The position involves batch record review of manufacturing and testing protocols, monitoring GMP-compliant documentation, and preparation of batch-specific batch record review reports.

Requirements

• Scientific training or studies
• GMP knowledge and pharmaceutical documentation requirements
• Experience in serialization
• Good communication skills
• Interest in reviewing documents and identifying discrepancies
• Strong sense of responsibility and quality-oriented approach

Benefits

• Flexible working hours
• 30 days' vacation
• Comprehensive training opportunities
• Modern working environment
• JobRad
• EGYM Wellpass
• Employee restaurant
• Regular events