As the Technical Writer within the Sleep & Respiratory Care portfolio, you will be creating/updating US and global instructions for use and labeling for regulated medical device products. Your role involves developing, updating, and maintaining labeling including instructions for use, online help files, device labeling, and packaging for medical devices. You will translate complex engineering, clinical, and regulatory inputs into clear, concise, user-focused content. You will also partner with experienced Technical Writers to develop expertise in medical device labeling requirements and support the creation and maintenance of labels, IFUs, and labeling plans throughout the product lifecycle.
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Job Type
Full-time
Career Level
Entry Level