CareerPlan

Assistenz (m/w/d) Zulassung

Saarbrücken, SAARLANDFull-time2026-08-25 → 2026-11-02

Core

Administrative and organizational support for regulatory affairs, including new product registrations, status monitoring, and document management for pharmaceuticals and medical devices.

Role type

Administrative Assistant (Regulatory Affairs)

Builds

Regulatory documentation and registration dossiers for pharmaceuticals and medical devices

Domain

Pharmaceuticals and Medical Devices

Deliverable

dashboards & analysis

Required skills

Regulatory affairs knowledge, MS Office, document management systems, deadline management, database management

Preferred skills

Chemistry or pharmaceutical industry background, Spanish language skills

Technologies

MS Office, document management systems

Responsibilities

Coordinate and manage regulatory documents and databases, monitor registration deadlines, communicate with international authorities and partners, maintain product information texts

Seniority

Entry-level to Junior