Medical Device Labeling Manager | Technical Writing Leader

USA-Medtronic MiniMed, Inc 1017; Los Angeles (CA); On-site; USD 107,000 - 183,000; Full time

Benefits offered by this job

Health, dental and vision insurance

401(k) with company match

Paid time off

Job summary

MiniMed in Los Angeles seeks a Technical Writing Manager to lead a team responsible for writing, editing and document control for medical device labeling, partnering with Program Management, Regulatory Affairs and Change Management to ensure timely, compliant content for worldwide launches.

The ideal candidate brings regulated industry expertise, strong leadership, and a passion for building high‑performing teams while delivering labeling that meets FDA, EU MDR and ISO requirements, ultimately

Qualifications

• Bachelor’s Degree with 5+ years in technical writing or labeling in medical device or regulated industry.
• Advanced Degree with 3+ years in technical writing or labeling in a regulated field.
• Familiar with FDA, EU MDR and ISO labeling requirements.

Responsibilities

• Manages a team of technical writers and project coordinators responsible for labeling content.
• Partner with Program Management and Regulatory Affairs to align labeling timelines with product launches.
• Collaborate with Change Analyst team on documentation changes and change orders.
• Execute team goals aligned to OKRs and company priorities.
• Apply best practices in labeling writing and ensure compliance.

Skills

Technical leadership

Technical writing

Regulatory knowledge

Medical device labeling

Education

Bachelor's Degree in a relevant field

Advanced Degree

Tools

CMS

Job description

MiniMed in Los Angeles seeks a Technical Writing Manager to lead a team responsible for writing, editing and document control for medical device labeling, partnering with Program Management, Regulatory Affairs and Change Management to ensure timely, compliant content for worldwide launches.

The ideal candidate brings regulated industry expertise, strong leadership, and a passion for building high‑performing teams while delivering labeling that meets FDA, EU MDR and ISO requirements, ultimately