Sr. Technical Writer (New Kensington, PA)

What you’d do

Create and update instructions for use and labeling for regulated medical devices in the Sleep & Respiratory Care portfolio. Lead labeling strategy for new products and post-market changes, and support audits and regulatory submissions. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• Bachelor's in technical writing or similar with 2+ years experience, or Master's degree
• Medical device labeling and instructions for use experience
• Translate engineering, clinical, regulatory inputs into clear content
• Labeling project management
• Support audits and regulatory submissions