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Technical Writer
Irvine, California, United States
$68k-$96k/yr OnsiteFull Time
3+ YOEBachelor's degree in a related field and 3 years technical writing experience (or equivalent), experience in biotech/medical device preferred, strong editing/proofreading, and familiarity with technical documentation tools and Microsoft Office.
MedCap Flare, Adobe, Paligo, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Publisher, Photoshop
2mo
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Technical Writer I
Irvine, California, United States
OnsiteFull Time
1+ YOE1+ years of technical writing experience; strong writing/editing; ability to explain complex information clearly; detail-oriented; able to work independently.
Markdown, Confluence, API Documentation
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Technical Writer - Onsite
Irvine, California, United States
$68k-$102k/yr OnsiteFull Time
2+ YOEBaccalaureate degree and minimum 2 years medical device regulatory/product compliance, labeling, or technical writing experience; knowledge of medical device regulations; strong writing and editing skills.
Adobe InDesign, Adobe Acrobat, Photoshop, Adobe Illustrator, XML, HTML, CMS
2w
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Technical Writer - Onsite
Irvine, California, United States
$68k-$102k/yr OnsiteFull Time
2+ YOEBaccalaureate degree and minimum 2 years regulatory/product compliance, labeling, technical writing, or editing in medical devices; knowledge of US/EU medical device regulations and risk standards; proficiency with Adobe InDesign, structured authoring, and CMS.
Adobe InDesign, Adobe Acrobat, PhotoShop, Adobe Illustrator, XML, HTML, CMS, Product Lifecycle Management (PLM)
2mo
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Senior Technical Writer
Costa Mesa, California, United States
$146k-$194k/yr OnsiteFull Time
7+ YOE7+ years of XML-based technical documentation, MIL-STD-40051, DOD experience; strong writing and project-management skills; eligible for Secret or higher clearance.
XML, MIL-STD-40051, RTX Eagle, Siemens Rapid Author, Rapid Author, Data Modules
2mo
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Technical Writer - Product Development (Dental Devices)
Irvine, California, United States
$30-$43/hr OnsiteFull Time
4+ YOEBachelor's degree in engineering or science; 4+ years direct documentation in medical device/technical industry; knowledge of 21 CFR 820 and US/international regulations for documentation; experience with regulatory submissions and quality systems.