The Senior Technical Writer creates and maintains end-user documentation for medical devices, ensuring compliance with FDA, ISO, and other regulatory standards.
With at least 5 years of experience in the medical device or life sciences industry, the candidate should be proficient in MadCap Flare and familiar with QMS and regulatory requirements.
The role involves managing complex documentation projects, contributing to process improvements, and providing technical leadership.
Strong communication, project management, and cross-functional collaboration skills are essential.
Preferred qualifications include knowledge of global labeling standards and experience with graphics and publishing tools.
Offering a competitive salary range of $90,100-$153,300/year, along with comprehensive benefits, the position suits candidates seeking a challenging and rewarding career in a dynamic environment.