Senior Batch Record Specialist | Senior Batch Record (w/m/d)
Brunel GmbH NL Mannheim
Job Summary
As a Senior Batch Record Specialist, you will play a critical role in ensuring pharmaceutical production excellence. Your day-to-day responsibilities include reviewing and processing batch documentation in strict compliance with GMP standards, managing manufacturing instructions, and coordinating corrections with production teams. You will act as a key support figure during GMP audits and inspections, while also taking ownership of SOP creation and staff training. A significant part of your role involves analyzing batch data to identify process optimizations and supporting the implementation of Electronic Batch Record (EBR) systems. This position is ideal for a professional with a background in biotechnology who thrives in a regulated environment, values process improvement, and enjoys cross-functional coordination. The role offers a stable, long-term career path with a focus on professional development and a collaborative company culture.
Required Skills
Education
Master's degree in Biotechnology or a comparable field.
Experience
- Several years of professional experience in the manufacturing of parenterals.
- Proven experience in GMP-compliant documentation and pharmaceutical hygiene standards.
- Professional experience in cross-functional coordination and process improvement.
- Experience in the implementation or maintenance of electronic documentation systems (EBR/MES).
Languages
Additional
- Not specified
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