Documentation Specialist (m/w/d) in Teilzeit
Core
Creating technical documentation for surgical instruments in compliance with MDR (2017/745) and coordinating documentation processes across product lines.
Role type
Documentation Specialist
Builds
Technical documentation for surgical instruments
Domain
Medical Devices / Regulatory Affairs
Required skills
MDR (2017/745) knowledge, PLM systems (Windchill), Microsoft 365, English (fluent), project coordination, audit support
Preferred skills
Medical device engineering background, Regulatory Affairs experience
Responsibilities
Creating technical documentation for surgical instruments, Coordinating documentation tasks across departments, Managing documentation within development projects, Supporting international regulatory approval projects, Participating in audits by notified bodies
Seniority
Mid-level, hands-on IC
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