I'm currently looking for a Technical Writer to join a world‑class Global Device Engineering team
In this hybrid role, you'll be responsible for the design and development of operator manuals, device labelling, and user instructions that meet the highest clarity and compliance standards in the medical device industry.
You will collaborate closely within a cross-functional team (with Regulatory Labelling, Quality, Clinical, Human Factors, Commercial, Engineering, Regulatory etc.) to optimize medical device labelling clarity and completeness.
Experience needed:
* Proven experience in technical writing / Labelling design (medical device experience preferred)
* Exceptional writing/editing skills & medical device regulatory knowledge
* Proficiency with Adobe Creative Suite, MS Office; MasterControl is a plus
* The skill to turn Technical jargon into user friendly language