Rédacteur technique médical — Documentation & Conformité

Medtronic plc; Mounds View (MN); On-site; USD 68,000 - 102,000; Full time

Benefits offered by this job

Health insurance

Dental and vision insurance

401(k) with match

Paid time off

Tuition assistance

Employee stock purchase plan

Job summary

Medtronic plc in the United States (Mounds View, MN) is seeking a Technical Writer to develop customer-facing product documentation, including labeling, user guides, and IFUs for cardiovascular devices. The role requires distilling complex technical content for clinicians and patients, coordinating reviews, and ensuring compliance with Medtronic design standards.

The candidate will work with cross-functional teams, participate in regulatory submissions, and manage translation processes while

Qualifications

• Bachelor's degree required; minimum 2 years in communications, labeling, and/or technical writing
• Experience in medical device labeling and regulatory-friendly documentation preferred
• Experience with XML content and content management systems is beneficial

Responsibilities

• Plan, develop, and write medical device labeling and related documentation.
• Create customer-facing manuals and instructions for use (IFUs).
• Coordinate translations and track translation status.
• Ensure content complies with quality systems and regulatory standards.
• Collaborate with cross-functional teams for input and reviews.

Skills

Technical writing

Medical device labeling

XML authoring

Regulatory knowledge

Cross-functional collab

Education

Bachelor's degree

Advanced degree

Tools

Azure DevOps

Windchill

Paligo

MadCap

Author-it

Job description

Medtronic plc in the United States (Mounds View, MN) is seeking a Technical Writer to develop customer-facing product documentation, including labeling, user guides, and IFUs for cardiovascular devices. The role requires distilling complex technical content for clinicians and patients, coordinating reviews, and ensuring compliance with Medtronic design standards.

The candidate will work with cross-functional teams, participate in regulatory submissions, and manage translation processes while