We are looking for a proactive, precise, and strong communicator to join our team as a Technical Writer in the medical device field.In this role, you will be responsible for delivering high-quality, compliant user documentation that supports the safe and effective use of our products and meets strict regulatory requirements.You'll work at the intersection of engineering, regulatory, and product, transforming complex information into clear, structured, and user-focused content.What You'll DoCreate, update, and manage user manuals and technical documentation in accordance with applicable regulationsEnsure documentation is clear, consistent, and aligned with usability and risk management requirementsCollaborate closely with R&D;, Regulatory Affairs, and Product ManagementGather and structure information from SMEs, engineering documents, and risk filesContribute to structured authoring and CCMS-based documentation (modular, topic-based, single-source)Manage the full documentation lifecycle: versioning, change control,



and traceabilityCoordinate localization processes with external translation partnersPrepare and publish documentation for digital distributionSupport audits and regulatory submissionsWhat We're Looking ForBachelor's or Master's degree in Humanities, Engineering, or a related STEM fieldAt least 2 years of experience in technical writing (ideally within a regulated environment)Fluent written and spoken English (additional languages are a plus)Excellent communication skills: clear, structured, and precise writing is essentialStrong ability to work cross-functionally and proactively gather informationExperience with a CCMS (Paligo is a plus)Solid understanding of structured authoring methodologies (topic-based writing, modular content, single-source publishing)Mandatory Technical SkillsAdvanced proficiency in Microsoft Office (Word & Excel) — essential for authoring, formatting, and document managementWorking knowledge of Adobe tools (InDesign, PDF suite) for layout, publishing, and final document preparationExperience in the medical device industryFamiliarity with regulatory frameworks (MDR, ISO *****, FDA)Knowledge of Adobe Illustrator or similar tools for graphics#J-*****-Ljbffr

📌 Technical Writer (Medical Devices) (Lazio)
🏢 Cosmed - The Metabolic
📍 Lazio