Senior Batch Record Specialist | Senior Batch Record (w/m/d)

Job Summary

As a Senior Batch Record Specialist, you will be responsible for the meticulous review and processing of batch documentation within a high-stakes pharmaceutical environment. Your daily activities will involve ensuring strict compliance with Good Manufacturing Practice (GMP) standards, controlling manufacturing instructions, and coordinating corrections across production units. You will play a pivotal role in supporting GMP audits, updating Standard Operating Procedures (SOPs), and conducting staff training. This position is highly collaborative, requiring you to act as a cross-departmental interface to reduce backlogs and drive process improvements. A unique aspect of this role is the opportunity to contribute to the implementation of new Electronic Batch Record (EBR) systems. This is an attractive opportunity for professionals seeking a permanent contract with a stable engineering service provider that offers comprehensive benefits, including 30 days of vacation and employer-funded pension schemes.