Technical Writer

Summary

I am an experienced Technical Writer / Regulatory Affairs Specialist who specializes in preparing submissions and maintaining technical documentation in order to remain in compliance with applicable regulatory requirements when bringing medical devices to market.

Expectations

I would like to work with a company that has a regulatory affairs team.

Work in United States

Employment Preferences

Expected Base Salary

**,000 USD

Academic Degree

Experience

Skills

• Technical Writer
• Medical Devices
• Regulatory Affairs Specialist
• K
• CE Mark
• Documentation
• Quality Management System
• SOP