Pharmazeutischer Assistent Robocell (m/w/d)

Roche

Mannheim, Germany
Gmp-compliant documentation
Batch review responsibilities
Deviation and capa management
The role supports the Asset Lead in ensuring GMP-compliant documentation and managing batch reviews for sterile drug manufacturing

Job Summary

  • The role supports the Asset Lead in ensuring GMP-compliant documentation and managing batch reviews for sterile drug manufacturing.
  • Candidates will lead continuous improvement projects and handle complex deviations including root cause analysis and CAPAs.
  • Roche offers a culture of personal expression and diverse benefits to help employees thrive personally and professionally.

Matching Summary

The role supports the Asset Lead in ensuring GMP-compliant documentation and managing batch reviews for sterile drug manufacturing.

Skills & Requirements

Must-have

  • GMP-compliant documentation
  • Batch review responsibilities
  • Deviation and CAPA management
  • SOP and instruction creation
  • Regulatory inspection participation

Nice-to-have

  • Lean methodology experience
  • Innovative technology implementation
  • Interdisciplinary thinking skills
  • Conflict resolution abilities

Key Requirements

  • Degree in Pharmacy or natural sciences
  • Multi-year pharmaceutical industry experience
  • Advanced German and English language skills
  • Experience with AMWHV and AMG regulations

Work Rights

Not specified

Tailored Resume

Cover Letter