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Contract Technical Writer

  • Contract Technical Writer job type Posted on: Nov 03, 2026
  • Contract Technical Writer experience level Grove Technical Resources
  • Contract Technical Writer employment type Lafayette, Colorado
  • Contract Technical Writer employment type Onsite
  • Contract Technical Writer salary Full-time
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Job Title :

Contract Technical Writer

Job Type :

Full-Time

Job Location :

Lafayette Colorado United States

Remote :

No

Jobcon Logo Job Description :

View Full Description
We're Hiring: Technical Writer – Medical DeviceLocation: Lafayette, CO (Hybrid – 3–4 days onsite)Duration: 6 Months (Nov 2026 – Apr 2027)Type: W2 contractWork Schedule: 40 hours/weekEducation: Bachelor's DegreeExperience: 5+ YearsKey Responsibilities:Develop and maintain Instructions for Use (IFUs) and electronic IFUs (eIFUs).Create and manage structured XML-based technical documentation.Work with CMS platforms and publishing workflows.Perform documentation change impact analysis and support translation/localization processes.Collaborate with R&D, Regulatory, and Quality teams.Must-Have Skills:Adobe FrameMaker / Structured FrameMakerStructured Authoring (XML, HTML, DITA)CMS-based Content ManagementMedical Device IFU DocumentationQuality System Processes and Change Impact AnalysisNice to Have:Adobe InDesign, Illustrator, PhotoshopVasont CMSMedical Device / Regulated Industry Experience.

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Jobcon Logo Position Details

Posted:

Nov 03, 2026

Reference Number:

10440_4484399365

Employment:

Full-time

City:

Lafayette

Job Origin:

APPCAST_CPC

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We're Hiring: Technical Writer – Medical DeviceLocation: Lafayette, CO (Hybrid – 3–4 days onsite)Duration: 6 Months (Nov 2026 – Apr 2027)Type: W2 contractWork Schedule: 40 hours/weekEducation: Bachelor's DegreeExperience: 5+ YearsKey Responsibilities:Develop and maintain Instructions for Use (IFUs) and electronic IFUs (eIFUs).Create and manage structured XML-based technical documentation.Work with CMS platforms and publishing workflows.Perform documentation change impact analysis and support translation/localization processes.Collaborate with R&D, Regulatory, and Quality teams.Must-Have Skills:Adobe FrameMaker / Structured FrameMakerStructured Authoring (XML, HTML, DITA)CMS-based Content ManagementMedical Device IFU DocumentationQuality System Processes and Change Impact AnalysisNice to Have:Adobe InDesign, Illustrator, PhotoshopVasont CMSMedical Device / Regulated Industry Experience.

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