responsible for producing high quality documentation, appropriate to its intended audience.
ensure that development and delivery of documentation is consistent and compliant with regulatory and company guidelines.
work with internal teams to obtain an in-depth understanding of the product(s).
apply existing standard instructions for use content as well as potential new content with a strong focus on reuse and single-source opportunities.
write, and edit instructions for use for medical device immunoassays and chemistry assays customer-facing documentation using an XML content management system ensuring all writing project plan deliverables are met.
Requirements
Minimum 5 years' direct work experience technical writing in a medical device manufacturing company.
Expert skill level using current versions of standard authoring tools, including experience with XML-based content management system, Adobe Frame Maker and Adobe InDesign (intermediate level).
Previous experience writing in a medical device or other regulated industry.
Scientific background is a plus.
Technical Writing Certification (preferred) or equivalent.
Bachelor's degree in technical writing, business, science or other related field required.
Experience in standard business applications including electronic document control, word processing, spreadsheets and databases.
Benefits
medical insurance
dental insurance
vision insurance
401(k) retirement plan
life insurance
long-term and short-term disability insurance
paid parking/public transportation
paid time off
paid sick and safe time
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.