Specialist Batch Record Review | Spezi­a­list Batch Record Review (w/m/d)

Job Summary

This role involves ensuring the highest standards of documentation and quality control within a pharmaceutical manufacturing environment. The Specialist will be responsible for creating and revising SOPs, supporting GMP audits, and meticulously reviewing and processing batch records. A key part of the role includes electronic data capture and analysis, contributing to continuous process improvement, and conducting internal training sessions. This position is ideal for a detail-oriented professional with a strong background in pharmaceutical production and a deep understanding of GMP regulations, looking for a challenging role in a growing company that values professional development and offers a permanent contract.