CareerPlan

Technischer Redakteur für Pharmaanlagen (m/w/d)

Gladenbach, HESSENFull-time2026-10-21 → 2026-11-11

Core

Technical documentation for new pharmaceutical installations and modifications, ensuring compliance with regulatory requirements and integrating safety warnings.

Role type

Technical Editor (Pharmaceutical Engineering)

Builds

Operational and user manuals, process and design documentation, safety warnings.

Domain

Pharmaceutical industry, cGMP-regulated environment.

Required skills

Technical documentation, regulatory compliance (cGMP), template development, cross-functional coordination, translation management.

Preferred skills

Experience with editorial systems, project implementation or optimization.

Technologies

Editorial systems.

Responsibilities

Create and maintain operational and user manuals, define and integrate safety warnings, ensure compliance with normative and legal requirements, coordinate editorial reviews with technical departments and customers.

Seniority

Mid-level, hands-on IC.