Why this role Floaid is finalizing documentation for a new platform. We need a hands‑on technical writer who can rapidly bring our User/Operator Manual, Service & Maintenance Manual, Installation & Commissioning Guide, and related controlled documents to release quality under a medical‑device QMS. Employment: Contract (6 months) with option to extend or convert to full‑time What you’ll own (deliverables) Operator Manual (IFU): setup, priming, alarms, operating modes, UI walkthroughs, cleaning/sterilization, warnings/contraindications, symbol glossary (ISO 15223‑1), and labeling content. Service & Maintenance Manual: scheduled PM, test points, calibration procedures, fault codes, troubleshooting trees, disassembly/reassembly with torque specs, ESD and safety controls, spares & consumables lists, and exploded‑view diagrams. Installation & Commissioning Guide (Site‑Ready): facilities requirements, power/EMC/grounding, acceptance checklists, and verification steps. Field Bulletins & Work Instructions: change summaries (ECOs), retrofit kits, service advisories, and controlled WIs. Verification/Validation Documentation Support: author/format protocols & reports (e.g., endurance, hemolysis, performance curves), acceptance criteria tables, and traceability to requirements. Software Release Notes & UI Text Styleguide: error/alert taxonomy, revision history, and string conventions. Training Collateral: quick‑start guide, competency checklists, and slide handouts. Document Package Readiness: version control, approval routes, printable and web‑optimized PDFs, and source files (structured authoring). Responsibilities Plan a documentation roadmap to reach DHF/DMR‑ready status; estimate effort, risks, and dependencies. Interview engineers, clinical advisors, and service teams; convert tribal knowledge into clear, controlled content. Create procedures that are step‑by‑step, testable, and cross‑referenced with hazards, warnings, and PPE/ESD icons. Build troubleshooting flows for alarms/fault codes (symptom → probable cause → diagnostic steps → remedy). Generate/curate diagrams from CAD or photos; annotate assemblies and connectors; maintain consistent numbering schemes. Ensure regulatory alignment with ISO 13485 documentation controls, ISO 14971 risk controls/IFU warnings, IEC 60601‑1 & 60601‑1‑2 safety/EMC references, IEC 62304 software notes, IEC 62366 usability, and Indian CDSCO expectations. Drive reviews (RACI) and manage redlines; maintain change history, doc numbers, and revisions. Prepare documents for localization; manage variables, units, and terminology consistency. Must‑have qualifications Passion for technical writing. Working knowledge of ISO 13485, ISO 14971, IEC 60601‑1/‑1‑2, IEC 62304, IEC 62366, and ISO 15223‑1symbols. Experience writing to DHF/DMR standards with traceability to product requirements and risk controls. Strong ability to read schematics, wiring diagrams, and mechanical assemblies; comfortable with test instruments and fixture procedures. Fluency in structured authoring (DITA or equivalent) and controlled docs (templates, numbering, TOC/LOT/LOF, revision control). Excellent visual communication: creating exploded views, callouts, and troubleshooting trees. Superb written English suitable for clinicians and biomeds; clear, concise, and audit‑ready.

About FLOAID MEDTECH

We, “Floaid Medtech” is an evolving venture aiming towards the development of cutting edge medical devices, motivated with “Make In India” vision. Our own vision is to provide state of the art medical technology to our nation, homegrown with international standards, at affordable prices. J