QA Manager (GMP Environment) | QA-Manager (m/w/d) GMP-Umfeld

Job Summary

This critical role seeks a professional to manage and continuously optimize quality assurance systems within a strict Good Manufacturing Practice (GMP) environment, ensuring full compliance with current pharmaceutical guidelines. The QA Manager will be responsible for coordinating quality-relevant problem-solving, planning laboratory activities, and actively participating in analytical lifecycle management tasks. A primary focus is ensuring the timely, GMP-compliant execution and meticulous documentation of quality checks for pharmaceutical products. Key daily activities include the creation, review, and release of critical operational documents, including Standard Operating Procedures (SOPs), master documents, and production records. The successful candidate must possess a background in natural sciences or a related technical field, practical experience in QA/QC, and strong knowledge of GMP regulatory requirements. This position is essential for maintaining high quality standards and involves preparing for and supporting external audits and regulatory inspections.