Location: Bangalore, Karnataka, India
Job Type: Full-Time
Work Mode: Fully Onsite
Department: Research & Development
Experience Required: 0–3 Years
Industry: Life Sciences | Medical Devices | In Vitro Diagnostics (IVD)
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in serving science, helping healthcare and research organizations accelerate innovation, improve patient diagnostics, and enhance laboratory productivity. With billions invested annually in research and development, the company empowers professionals worldwide to contribute toward groundbreaking scientific advancements and healthcare solutions.
If you are looking to build a career in technical documentation, regulatory labeling, medical devices, or life sciences content management, this opportunity offers exposure to global quality standards, cross-functional collaboration, and regulated documentation environments.
Job Overview – Technical Writer (Labeling)
Thermo Fisher Scientific is hiring a skilled and detail-oriented Technical Writer – Labeling for its Bangalore office. The selected candidate will be responsible for creating, reviewing, updating, and maintaining labeling content and packaging documentation aligned with global regulatory and quality standards.
This role is ideal for candidates with prior experience in technical writing, regulatory documentation, labeling operations, medical device documentation, or IVD product documentation within regulated pharmaceutical and healthcare industries.
Key Responsibilities
Create, review, and update product labels and packaging artwork based on regulatory and business requirements.
Ensure all documentation complies with QSR, ISO standards, QMS procedures, and internal regulatory policies.
Maintain consistency with approved company templates, style guides, and documentation frameworks.
Collaborate with cross-functional departments including:
Product Development
Regulatory Affairs
Quality Assurance
Marketing
Global Operations
Manage multiple documentation and labeling projects in a fast-paced global environment.
Support deviation management, CAPA activities, and complaint investigations through documentation expertise.
Contribute toward continuous improvement of labeling workflows, templates, and documentation systems.
Verify technical accuracy and regulatory compliance across labeling deliverables.
Eligibility Criteria
Educational Qualification
Bachelor’s degree in:
Life Sciences
Biotechnology
Pharmacy
Biomedical Sciences
Microbiology
Related scientific discipline
Relevant industry experience may also be considered.
Experience Required
0–3 years of experience in:
Label creation
Technical writing
Medical device documentation
IVD documentation
Regulatory labeling
Controlled documentation management
Preferred Industry Experience
Life Sciences
Medical Devices
In Vitro Diagnostics (IVD)
Healthcare Documentation
Required Skills
Strong English communication, writing, editing, and proofreading skills.
Knowledge of QSR, ISO standards, and Quality Management Systems (QMS).
Ability to manage documentation within regulated global environments.
Familiarity with documentation workflows and change control processes.
Experience handling technical and regulatory content accurately.
Preferred Technical Skills
Hands-on experience with:
Adobe InDesign
Adobe Illustrator
Visual documentation tools
Label design software
Understanding of:
EU IVDR requirements
Medical device labeling regulations
Regulatory documentation standards
Additional Preferred Skills
Multilingual communication skills such as:
German
French
Spanish
Swedish
Strong collaboration and stakeholder communication abilities.
High attention to detail and process-driven mindset.
Ability to work independently as well as within global teams.
Interest in understanding complex scientific products and systems.
Knowledge of EU MDR regulations will be considered an added advantage.
Why Join Thermo Fisher Scientific?
Opportunity to work with one of the world’s leading life sciences companies.
Exposure to global regulatory documentation and labeling standards.
Collaborative international work environment.
Career growth opportunities in technical writing, regulatory affairs, labeling operations, and quality documentation.
Contribute to scientific innovations that positively impact healthcare and patient safety globally.
Who Should Apply?
This opportunity is highly suitable for:
Technical Writers in Life Sciences
Regulatory Documentation Professionals
Medical Device Documentation Specialists
IVD Labeling Professionals
Pharmacy and Biotechnology Graduates with labeling experience
Quality Documentation Executives
Apply Now
Candidates interested in building a long-term career in technical writing, regulatory labeling, and life sciences documentation are encouraged to apply for this opportunity at Thermo Fisher Scientific, Bangalore.
Stay connected with ThePharmaDaily.com for the latest global pharmaceutical, clinical research, pharmacovigilance, biotechnology, medical writing, and regulatory affairs job updates.
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