Vacancy Description
We are seeking a qualified Technical Writer (Medical Devices) to join an international division and collaborate with senior engineers and technicians worldwide.
Key Responsibilities
- Edit and maintain technical documentation in a regulated environment (medical devices).
- Manage and update documents across their lifecycle (review, approval, release).
- Support document management systems (e.g., Windchill), including workflows for review and approval.
- Act as first‑level support for documentation tools and processes (user guidance, issue resolution).
- Maintain document repositories and ensure alignment between different storage systems.
- Create and manage:
- Glossaries and reference lists
- Redlines and document updates per product increment
Required Skills & Experience
- Proven experience as Technical Writer / Documentation Specialist.
- Experience in regulated envir...
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Submit your application for Tecnical Writer (Medical Devices) International Project. (Cádiz) at ALTEN Delivery Centre Spain
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