Sachbearbeitung Arzneimittelzulassung (m/w/d)
Core
Supporting Regulatory Affairs Managers and CMC Coordinators in the global creation, consolidation, and submission of drug approval documents.
Role type
Administrative specialist for drug regulatory submissions
Builds
Global drug approval documentation packages
Domain
Pharmaceutical industry / Regulatory Affairs
Deliverable
client delivery
Required skills
Document management, global correspondence, software proficiency (DocuBridge), translation coordination, administrative task execution
Preferred skills
Certified Pharmaceutical Reference (Geprüfter Pharmareferent), natural sciences background (Chemical Lab Assistant, Chemical-Technical Assistant, or Pharmaceutical-Technical Assistant), first experience in pharma industry, fluent English, MS Office proficiency
Technologies
DocuBridge, MS Office
