Job 142364

Honeywell

**
Trackwise manufacturing (mes)
Trackwise quality (qms)
Gxp-regulated environments
** Honeywell is seeking an experienced Senior Technical Writer with expertise in regulated Life Sciences software to join their TrackWise product documentation team. The role involves managing the documentation lifecycle for TrackWise Manufacturing and Quality solutions, ensuring content is technically accurate and regulatory-compliant. **

Job Summary

  • Own the end-to-end documentation lifecycle for TrackWise Manufacturing (MES) and TrackWise Quality (QMS), producing technically accurate, regulatory-aware, and useful content for pharmaceutical and biotech customers.
  • Plan, write, and maintain installation guides, configuration manuals, user guides, release notes, API documentation, and validation support packages (VSPs), including GxP-relevant documentation.
  • Lead structured knowledge-gathering sessions with SMEs and facilitate content reviews, collaborating with UX, Customer Success, and Implementation teams to ensure alignment and address documentation gaps.

Matching Summary

Match Score: 75

** Honeywell is seeking an experienced Senior Technical Writer with expertise in regulated Life Sciences software to join their TrackWise product documentation team. The role involves managing the documentation lifecycle for TrackWise Manufacturing and Quality solutions, ensuring content is technically accurate and regulatory-compliant. **

Skills & Requirements

Must-have

  • TrackWise Manufacturing (MES)
  • TrackWise Quality (QMS)
  • GxP-regulated environments
  • DITA or MadCap Flare
  • topic-based authoring

Nice-to-have

  • mentoring junior colleagues
  • actionable solutions and innovation
  • smarter, safer and more sustainable

Key Requirements

  • Minimum 3 years of technical writing experience
  • At least 2 years in Life Sciences software
  • Bachelor's degree or higher
  • Strong portfolio of technical documentation samples

Work Rights

Not specified

Tailored Resume

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