Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Technical Writer – Manuals

Thermo Fisher Scientific
3-4 years
Not Disclosed
Bangalore, India
2 May 21, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

Technical Writer – Manuals

Company: Thermo Fisher Scientific
Job Title: Technical Writer – Manuals
Job ID: R-01351899
Location: Bengaluru, Karnataka
Job Category: Research & Development / Technical Documentation
Employment Type: Full-time
Work Mode: Fully On-site
Work Schedule: Monday – Friday (Standard Office Hours)


Job Summary

Thermo Fisher Scientific is hiring a Technical Writer – Manuals to create, maintain, and improve technical documentation for scientific instruments, software products, and regulated life sciences products. The role focuses on technical writing, regulatory-compliant documentation, cross-functional collaboration, translation coordination, and documentation process improvement.


Key Responsibilities

  • Develop, update, and proofread:

    • Instrument User Manuals

    • Software User Manuals

    • WebHelp documentation packages

    • Technical product documentation

  • Convert complex scientific, technical, and regulatory content into clear user-friendly documentation.

  • Improve documentation quality including:

    • Text

    • Layout

    • Images

    • Formatting

  • Ensure compliance with:

    • QSR

    • ISO standards

    • Internal quality systems

    • Regulatory documentation standards

  • Coordinate with translation agencies and internal teams for localization and document translation.

  • Follow company:

    • Style guides

    • Templates

    • Quality Management System (QMS)

  • Collaborate with:

    • Product Development

    • R&D

    • Regulatory Affairs

    • Quality Assurance

    • Marketing

    • Global Operations

  • Support:

    • Deviation investigations

    • CAPA activities

    • Complaint investigations

  • Drive continuous improvement of documentation standards and workflows.

  • Manage multiple technical documentation projects.


Required Qualifications

  • Bachelor’s or Master’s Degree in:

    • Technical Communication

    • English

    • Journalism

    • Life Sciences

    • Biology

    • Biochemistry

    • Molecular Biology

    • Related fields

Equivalent experience may also be considered.


Required Experience

  • 3–4 years of technical writing experience

  • Industry background in:

    • Life Sciences

    • Medical Devices

    • IVD (In Vitro Diagnostics)

Experience with:

  • Regulated documentation

  • User manuals

  • Scientific product documentation