Sachbearbeiter Zulassungen Parallelimport (m/w/d)
Core
Managing approval procedures for parallel distribution/import of pharmaceuticals, maintaining existing approvals, and creating packaging materials.
Role type
Regulatory Affairs Specialist (Pharmaceuticals)
Builds
Regulatory approvals and packaging materials for pharmaceutical products
Domain
Pharmaceuticals / Regulatory Affairs
Required skills
Regulatory compliance, documentation management, stakeholder communication, data entry, packaging design
Preferred skills
MS Office, quality assurance
Technologies
MS Office, ERP systems
Responsibilities
Handling approval procedures for parallel distribution/import, maintaining existing approvals, creating packaging materials, communicating with authorities and brand owners, documenting and archiving regulatory documents