Senior Medical Device Labeling & Content Lead

ATR International; Irvine (CA); On-site; USD 110,000 - 170,000; Full time

Job summary

ATR International is seeking a Principal Technical Writer in Irvine, CA to lead labeling development for neurovascular medical devices. You will produce IFUs, user guides, electronic labeling, and packaging artwork, translating complex regulatory information into clear, user-focused content for clinicians, healthcare professionals, and patients.

The role requires 6+ years in medical devices labeling/technical writing, strong regulatory knowledge, and hands-on experience with InDesign and

Qualifications

• 6+ years in medical devices labeling and technical writing.
• Experience translating regulatory requirements into user-friendly content.
• Understanding of labeling standards and regulatory expectations.

Responsibilities

• Lead end-to-end labeling development (IFUs, user guides, electronic labeling).
• Ensure regulatory and quality compliance across global standards.
• Collaborate with R&D, Regulatory Affairs, QA, and Marketing to align content.

Skills

Medical devices experience

Technical writing

Labeling development

Adobe InDesign

Adobe Illustrator

Regulatory knowledge

Education

Master's in regulatory or engineering

Tools

Adobe InDesign

Adobe Illustrator

Content management systems

Job description

ATR International is seeking a Principal Technical Writer in Irvine, CA to lead labeling development for neurovascular medical devices. You will produce IFUs, user guides, electronic labeling, and packaging artwork, translating complex regulatory information into clear, user-focused content for clinicians, healthcare professionals, and patients.

The role requires 6+ years in medical devices labeling/technical writing, strong regulatory knowledge, and hands-on experience with InDesign and