Develop and maintain user-centric instructional materials for medical devices and software products
Collaborate with cross-functional teams to ensure compliance with regulatory standards and enhance user experience
Manage all phases of content development projects, including needs assessment, timelines, and content management
Required Qualifications
Bachelor's degree in a related field or equivalent experience
Minimum of 4 years of experience in content development
Functional knowledge of the medical device industry and regulatory affairs
Experience in writing for a global audience and working in a highly regulated environment
Demonstrated ability to work effectively in a team environment
Average salary estimate
$80000
/ YEARLY (est.)
min
max
$70000K
$90000K
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