Senior Medical Device Labeling Writer – Neurovascular

Regulatory Jobs; Irvine (CA); On-site; USD 85,000 - 127,000; Full time

Benefits offered by this job

Health, dental and vision insurance

401(k) with company match

Paid time off

Tuition assistance

Job summary

Medtronic in Irvine, CA seeks a Sr. Technical Writer - Labeling Content and Artwork Development to develop and maintain labeling content for neurovascular medical devices. The role collaborates with Regulatory, Quality, R&D, Clinical, and Marketing to ensure regulatory compliance and clear documentation.

The position follows an onsite work arrangement in Irvine, with no travel required. The ideal candidate translates complex technical information into user-focused labeling materials across the

Qualifications

• Bachelor's degree in a technical field or related discipline.
• 2+ years creating technical documentation in regulated environments.
• Experience translating clinical/engineering information into user-focused content.
• Experience with labeling content / artwork for medical devices preferred.

Responsibilities

• Develop, write, review, and maintain medical device labeling content (IFUs, labels, package inserts).
• Collaborate with Regulatory, Quality, R&D, Clinical, and Marketing to ensure accuracy and compliance.
• Create and manage artwork content for labeling components per design control processes.
• Interview SMEs to gather technical content and translate into clear documentation.
• Support labeling updates during product changes and regulatory submissions.

Skills

Technical writing

Labeling content

Artwork development

Cross-functional collaboration

Clear communication

Education

Bachelor's degree

Advanced degree (optional)

Tools

Document management systems

Job description

Medtronic in Irvine, CA seeks a Sr. Technical Writer - Labeling Content and Artwork Development to develop and maintain labeling content for neurovascular medical devices. The role collaborates with Regulatory, Quality, R&D, Clinical, and Marketing to ensure regulatory compliance and clear documentation.

The position follows an onsite work arrangement in Irvine, with no travel required. The ideal candidate translates complex technical information into user-focused labeling materials across the