Specialist Batch Record Review - Pharma | Specialist Batch Record Review - Pharma (m/w/d)

Job Summary

In this role, you will play a critical part in the pharmaceutical manufacturing process by ensuring the integrity and compliance of batch documentation. Your day-to-day responsibilities include reviewing batch manufacturing records for active ingredients, conducting in-process checks for biopharmaceutical products, and managing batch-related deviations. You will act as a key liaison between production departments and compliance officers, ensuring that all documentation meets GMP standards and internal SOPs. Additionally, you will coordinate the timely completion of documentation to support product release schedules and contribute to the continuous improvement of review checklists. This position is ideal for a detail-oriented professional with a background in life sciences who thrives in a collaborative, project-driven environment. You will be supported by a team dedicated to innovation and professional growth, working on high-impact projects within the pharmaceutical industry.