Label Specialist | Label Specialist (w/m/d)

Brunel GmbH NL Mannheim

Nordrhein-Westfalen, Deutschland
Published Feb 6, 2026
Full-time
Permanent

Job Summary

This role involves supporting a team by managing the end-to-end lifecycle of label designs, ensuring strict compliance with regulatory documentation and Good Manufacturing Practice (GMP) standards. The specialist will be responsible for coordinating label designs and translations according to current specifications, obtaining all necessary approvals, and maintaining comprehensive, traceable documentation. A key part of the job is communicating with external suppliers, conveying requirements, and assessing design proposals against specifications. This position is ideal for a professional with experience in pharmaceutical or medical device labeling, quality control, or clinical trial coordination, offering an opportunity to actively contribute to the harmonization of global, function-specific processes within a supportive corporate culture focused on professional development.

Required Skills

Education

Completed vocational training, e.g., Industrial Master Pharmacist, Pharmaceutical Technical Assistant (PTA), Medical Technical Assistant (MTA), Pharmaceutical Production Specialist (Pharmakant), or comparable qualification

Experience

  • Several years of professional experience in label design or in the manufacture/quality control of pharmaceuticals/medical devices
  • Alternatively, experience in the coordination or approval of clinical trials

Languages

English (Fluent)

Additional

  • Not specified