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
Healthcare / Pharmaceuticals
Required skills
Regulatory procedure management, Annual update/report preparation, Packaging material creation, Stakeholder communication, Documentation management, MS Office proficiency
Preferred skills
None stated
Technologies
MS Office
Responsibilities
Managing approval procedures for parallel distribution/import of pharmaceuticals, Maintaining existing approvals including Annual Updates and Reports, Creating and optimizing packaging materials for pharmaceuticals, Communicating with authorities and brand owners, Documenting and archiving regulatory documents
