Honeywell is seeking a Senior Technical Writer specializing in regulated Life Sciences software to enhance their TrackWise product documentation. The role involves managing the documentation lifecycle, collaborating with cross-functional teams, and ensuring high-quality content that meets regulatory standards for pharmaceutical and biotech clients
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.
Translate complex platform capabilities into clear documentation for administrators, operators, IT teams, and validation engineers, while overseeing and reviewing tasks performed by team members.
Plan, write, and maintain various types of documentation including installation guides, user guides, release notes, API documentation, and validation support packages, while collaborating with cross-functional teams.
Matching Summary
Match Score: 85
Honeywell is seeking a Senior Technical Writer specializing in regulated Life Sciences software to enhance their TrackWise product documentation. The role involves managing the documentation lifecycle, collaborating with cross-functional teams, and ensuring high-quality content that meets regulatory standards for pharmaceutical and biotech clients.
Skills & Requirements
Must-have
Regulated Life Sciences software
TrackWise Manufacturing (MES)
TrackWise Quality (QMS)
GxP-regulated environments
DITA or MadCap Flare
Topic-based authoring principles
Nice-to-have
Mentoring junior colleagues
ISA-88/ISA-95 workflows
21 CFR Part 11 controls
EU Annex 11 compliance
Electronic signature mechanisms
Key Requirements
Bachelor's degree or higher
Minimum 3 years technical writing experience
At least 2 years in Life Sciences software
Strong portfolio of technical documentation samples