Technical Writer Job at Thermo Fisher Scientific
Are you looking for a rewarding Technical Writer role in the global healthcare industry? This is an exciting Life Science Job at Thermo Fisher Scientific offering a unique opportunity for life science graduates to work on regulatory documentation and product labeling. If you have a passion for writing, science, and compliance, this role opens doors to a dynamic international career.
About the Company
Thermo Fisher Scientific is a global leader in scientific services and innovation, focused on enabling customers to make the world healthier, cleaner, and safer. The organization supports advancements in healthcare, environmental protection, food safety, and scientific research.
Job Details:
- Job Title: Technical Writer – Labeling
- Job ID: R-01350167
- Location: Bangalore, Karnataka, India
- Company: Thermo Fisher Scientific
- Job Type: Full-Time
- Category: Research & Development
- Work Mode: Fully Onsite
- Work Schedule: Monday – Friday
- Work Environment: Office
Role Overview
The Technical Writer – Labeling is responsible for creating and maintaining product labeling documentation in compliance with regulatory standards and internal quality systems. The role involves close collaboration with cross-functional teams to ensure technical accuracy, clarity, and consistency across labeling materials in a regulated global environment.
Key Responsibilities
- Create and update product labels and packaging content in alignment with regulatory requirements and internal procedures
- Ensure documentation complies with QSR, ISO standards, and internal Quality Management Systems (QMS)
- Follow company style guides, templates, and documentation standards
- Collaborate with Product Development, Regulatory Affairs, Quality Assurance, Marketing, and Global Operations teams
- Manage multiple documentation projects within assigned areas of responsibility
- Contribute to continuous improvement of documentation processes and standards
- Support deviation, CAPA, and complaint investigations with documentation expertise
- Ensure accuracy, clarity, and consistency in all labeling content
Qualifications & Experience
- Bachelor’s degree in Life Sciences or related field (or equivalent experience)
- 2–3 years of experience in labeling or technical writing within life sciences, medical devices, or IVD industry
- Strong English communication skills (writing, editing, and speaking)
- Experience working in regulated environments with global standards
Technical Skills
- Familiarity with tools such as Adobe InDesign and Illustrator for visual documentation
- Understanding of regulatory requirements such as EU IVDR
- Ability to manage multiple projects in a fast-paced environment
Preferred Skills
- Knowledge of additional languages (e.g., German, French, Spanish, Swedish) for localization
- Experience with EU MDR regulations (advantageous)
- Strong cross-functional collaboration and communication skills
- High attention to detail and accuracy
- Ability to work independently as well as in team settings
- Interest in understanding complex technical products and systems
