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

Brunel GmbH NL Mannheim

Mannheim, Baden-Württemberg, Deutschland
Published Feb 16, 2026
Full-time
Permanent

Job Summary

As a Batch Record Review Specialist, you will play a critical role in the quality assurance process of a growing pharmaceutical environment. Your daily responsibilities will center on the meticulous examination of batch documentation for finished medicinal products, bulk goods, and intermediates to ensure full compliance with AMG, AMWHV, and GMP standards. You will be responsible for identifying, evaluating, and tracking deviations in bulk production and packaging, while maintaining rigorous GMP-compliant documentation. Beyond administrative review, you will actively participate in operational quality tasks including conducting GEMBA walks, performing line clearances, and delivering specialized training. This position is ideal for detail-oriented professionals who thrive in regulated environments and are looking for a role that offers long-term stability, continuous professional development, and a collaborative company culture with a strong focus on employee appreciation and career progression.

Required Skills

Education

Completed vocational training in the pharmaceutical, chemical, or biological field (e.g., Pharmaceutical Technician, Chemical Laboratory Assistant, BTA, CTA) or a comparable qualification.

Experience

  • Professional experience in the pharmaceutical industry specifically focused on quality processes and deviation management.
  • Proven experience in the review of batch documentation and secure handling of GMP-compliant records.
  • Practical experience in conducting line clearances and operational quality audits.

Languages

German (Basic)

Additional

  • Permanent full-time contract; requires expertise in German pharmaceutical regulations (AMG, AMWHV).