Dokumentenmanagement- Und Trainingskoordinator (d/w/m)

Cytiva

Bad Kreuznach, Germany
Onsite
Document lifecycle control
Training role assignment
Quality management system improvement
Our work at Cytiva changes lives by accelerating the development and manufacturing of therapeutics

Job Summary

  • Our work at Cytiva changes lives by accelerating the development and manufacturing of therapeutics.
  • As a Document and Training Coordinator, you will be responsible for document and training management within modular technology, adhering to global corporate guidelines.
  • Cytiva offers opportunities for continuous personal and company development in an international environment within a fast-growing industry.

Matching Summary

Our work at Cytiva changes lives by accelerating the development and manufacturing of therapeutics.

Skills & Requirements

Must-have

  • Document lifecycle control
  • Training role assignment
  • Quality Management System improvement
  • Biotechnology
  • Pharmaceuticals
  • Engineering

Nice-to-have

  • Strong communication skills
  • Team player
  • Proactive initiative
  • Resilience
  • Structured work approach
  • Organizational talent

Key Requirements

  • Degree or comparable technical education
  • First professional experience in QA
  • Knowledge of QMS systems (Veeva Vault, SAP)
  • Fluent German
  • Good English

Work Rights

Not specified

Tailored Resume

Cover Letter