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Technical Writer Iii

Thermo Fisher Scientific
Thermo Fisher Scientific
4-5 years
upto 9 LPA
Bangalore, India
10 May 3, 2026
Job Description
Job Type: Remote Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Technical Writer III – Biosciences & Life Sciences Documentation Jobs in Bangalore | Thermo Fisher Scientific Careers 2026

Location: Thermo Fisher Scientific – Bangalore, Karnataka, India
Job Type: Full-Time
Work Mode: Fully Onsite
Department: Research & Development
Experience Required: Minimum 5+ Years of Experience
Eligibility: Experienced Professionals in Technical Writing, Biosciences, Life Sciences, Scientific Documentation, Regulatory Documentation, or Medical Writing


About Thermo Fisher Scientific

Thermo Fisher Scientific is one of the world’s leading scientific research and biotechnology organizations dedicated to helping customers accelerate life sciences research, improve diagnostics, solve analytical challenges, and enhance laboratory productivity worldwide.

With significant annual investments in research and development, the company empowers innovation across biotechnology, pharmaceuticals, healthcare, diagnostics, and scientific research sectors. Professionals joining Thermo Fisher Scientific gain exposure to advanced technologies, global scientific collaborations, and impactful healthcare solutions.


Technical Writer III Job Opening in Bangalore – Overview

Thermo Fisher Scientific is hiring an experienced Technical Writer III for its Bangalore office. This role is ideal for professionals passionate about scientific communication, bioscience documentation, regulatory content development, and technical content management within the life sciences industry.

The selected candidate will work closely with cross-functional teams including Research & Development, Product Management, Regulatory Affairs, Quality Assurance, and Scientific Experts to create and maintain high-quality technical documentation for advanced bioscience products and solutions.

This opportunity offers strong career growth for candidates experienced in technical writing, scientific documentation, XML/DITA authoring systems, and life sciences communication.


Key Responsibilities – Technical Writer III

  • Develop, edit, and maintain high-quality technical documentation for bioscience and life sciences products

  • Translate complex scientific and technical concepts into clear, concise, and user-friendly content

  • Collaborate with R&D, product management, quality assurance, and regulatory teams

  • Create structured content using XML/DITA-based authoring tools

  • Manage technical content within component content management systems

  • Ensure compliance with scientific, quality, and regulatory documentation standards

  • Continuously improve documentation processes and content accuracy

  • Handle multiple documentation projects while meeting strict timelines and quality standards

  • Maintain consistency in terminology, formatting, and scientific accuracy across documents

  • Support global scientific product documentation initiatives


Required Qualifications

  • Advanced Degree in Biosciences, Life Sciences, Biotechnology, Molecular Biology, Biomedical Sciences, or related disciplines

  • Minimum 5+ years of professional experience in Technical Writing or Scientific Documentation

  • Prior experience within the Bioscience, Biotechnology, Pharmaceutical, Healthcare, or Life Sciences industry preferred

  • Certification in Technical Writing will be considered an added advantage


Preferred Technical Skills

Candidates with expertise in the following areas will have an advantage:

  • XML/DITA Authoring Tools

  • Oxygen XML Editor / Oxygen XML Author

  • Component Content Management Systems (CCMS)

  • RWS Tridion Docs or similar platforms

  • Microsoft Office Suite

  • Adobe Creative Suite

  • Scientific and Regulatory Documentation Standards

  • Technical Editing and Structured Authoring

  • Cross-functional Collaboration and Documentation Lifecycle Management


Essential Skills Required

  • Excellent written and verbal communication skills

  • Strong scientific writing and documentation abilities

  • Exceptional attention to detail and accuracy

  • Ability to simplify complex scientific information

  • Strong project management and multitasking capabilities

  • Ability to work independently and collaboratively

  • Deadline-oriented mindset with strong organizational skills

  • Continuous learning attitude and willingness to update technical expertise


Why Join Thermo Fisher Scientific?

  • Opportunity to work with a globally recognized life sciences leader

  • Exposure to cutting-edge bioscience and biotechnology innovations

  • Collaborative and diverse work environment

  • Strong career growth and international exposure

  • Work on products and technologies impacting global healthcare and scientific advancement

  • Learn from industry experts in research, diagnostics, and scientific communication


Who Should Apply?

This opportunity is ideal for:

  • Experienced Technical Writers in Life Sciences

  • Bioscience Documentation Specialists

  • Medical Writers transitioning into technical documentation

  • Regulatory Documentation Professionals

  • Biotechnology and Pharmaceutical Industry Professionals

  • Scientific Communication Experts


Keywords for Job Seekers

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