The Technical Writer II is responsible for creating, revising, and maintaining technical documentation that meets Boston Scientific Quality System and global regulatory standards. This position focuses on developing clear, concise, and accurate design history file (DHF), risk management, and post-market surveillance documentation for interventional cardiology medical devices, ensuring that the documentation is accessible to various internal and external stakeholders.

Necessary requirements:

Education: 
Bachelors degree in English, English Teaching, Translation, Communications, Engineering, or similar.

Experience: 
2 years technical experience in a regulated industry, preferably in the medical device industry.

English Level: 
Advanced