SPECTRAFORCE
Job Title
Technical Writer Spec 2 Duration
12 months with possible extensions Location
San Diego, CA Employment Type
Contract Seniority Level
Mid-Senior level Base Pay Range
$44.00/hr - $49.50/hr Responsibilities
End-to-End Documentation:
Create and maintain user manuals, installation guides, and troubleshooting protocols for both customer-facing and internal use. Visual Communication:
Design illustrations, flow charts, and line art. Provide recommendations to engineers on optimizing data visualization to ensure clarity for the end user. Regulatory Compliance:
Ensure all content adheres to ISO standards, FDA requirements for Class II devices, and various country-specific regulatory submissions. Cross-Functional Collaboration:
Partner with Engineering, Quality Assurance, Regulatory Affairs, and Marketing to gather data and conduct IFU design reviews. Standards Leadership:
Develop and implement company-wide documentation standards and style guides to ensure global consistency. Project Management:
Manage complex documentation timelines within Agile development cycles and track changes through enterprise systems (SAP, Agile, GitHub). Qualifications
Experience:
5+ years of technical writing and editing for hardware/software (medical device or pharma experience is highly preferred). Regulated Industry Knowledge:
Extensive experience with regulatory compliance processes and medical device guidelines. DTP Tools:
MadCap Flare, Adobe FrameMaker, InDesign, or XML/DITA. Graphics:
Adobe Illustrator and Photoshop. Systems:
Familiarity with ERP (SAP/Oracle) and Version Control (GitHub/Perforce). Core Skills:
Ability to translate electro-mechanical concepts into concise prose; expert-level proofreading and editorial symbol usage.
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Technical Writer Spec 2 Duration
12 months with possible extensions Location
San Diego, CA Employment Type
Contract Seniority Level
Mid-Senior level Base Pay Range
$44.00/hr - $49.50/hr Responsibilities
End-to-End Documentation:
Create and maintain user manuals, installation guides, and troubleshooting protocols for both customer-facing and internal use. Visual Communication:
Design illustrations, flow charts, and line art. Provide recommendations to engineers on optimizing data visualization to ensure clarity for the end user. Regulatory Compliance:
Ensure all content adheres to ISO standards, FDA requirements for Class II devices, and various country-specific regulatory submissions. Cross-Functional Collaboration:
Partner with Engineering, Quality Assurance, Regulatory Affairs, and Marketing to gather data and conduct IFU design reviews. Standards Leadership:
Develop and implement company-wide documentation standards and style guides to ensure global consistency. Project Management:
Manage complex documentation timelines within Agile development cycles and track changes through enterprise systems (SAP, Agile, GitHub). Qualifications
Experience:
5+ years of technical writing and editing for hardware/software (medical device or pharma experience is highly preferred). Regulated Industry Knowledge:
Extensive experience with regulatory compliance processes and medical device guidelines. DTP Tools:
MadCap Flare, Adobe FrameMaker, InDesign, or XML/DITA. Graphics:
Adobe Illustrator and Photoshop. Systems:
Familiarity with ERP (SAP/Oracle) and Version Control (GitHub/Perforce). Core Skills:
Ability to translate electro-mechanical concepts into concise prose; expert-level proofreading and editorial symbol usage.
#J-18808-Ljbffr