Life Science Job at Thermo Fisher Scientific
Looking for a high-growth Life Science Job in a globally recognized healthcare company? Here is an exciting opportunity from Thermo Fisher Scientific for talented candidates seeking Technical Writer Jobs in Bangalore. This latest opening is ideal for professionals with experience in life sciences, labeling documentation, regulatory writing, and the medical device industry. If you are searching for an opportunity for life science graduates to work in a world-leading scientific organization, this role could be your next big career move. Explore eligibility, responsibilities, qualifications, and application details below.
About the Company
Thermo Fisher Scientific is a global leader in scientific research, healthcare, and laboratory solutions, committed to enabling customers to make the world healthier, cleaner, and safer. The organization supports innovation across life sciences, diagnostics, pharmaceuticals, and environmental sciences through cutting-edge technologies and scientific expertise.
Job Details:
- Job Title: Technical Writer – Labeling
- Location: Bangalore, Karnataka, India
- Job ID: R-01345230
- Company: Thermo Fisher Scientific
- Job Type: Full-time
- Category: Research & Development
- Work Mode: Fully Onsite
- Work Schedule: Standard (Monday–Friday)
Role Overview
The Technical Writer – Labeling will be responsible for creating and updating product labels and box print documentation in accordance with current regulatory requirements, quality standards, and market expectations. The role requires collaboration with multiple global teams to ensure technical accuracy, regulatory compliance, and consistency across labeling documentation.
The position also contributes to process improvement initiatives, quality documentation systems, and compliance activities within a regulated life sciences environment.
Key Responsibilities
- Create and maintain labels and box print documentation aligned with current procedures and regulatory requirements
- Ensure compliance with:
- QSR standards
- ISO standards
- Internal quality and regulatory requirements
- Follow company style guides, templates, and Quality Management Systems (QMS)
- Collaborate with cross-functional teams including:
- Product Development
- Regulatory Affairs
- Quality Assurance
- Marketing
- Global Operations
- Gather technical information and validate documentation accuracy
- Manage documentation activities within assigned responsibilities
- Support continuous improvement of documentation templates, standards, and processes
- Assist in:
- Deviation investigations
- CAPA activities
- Complaint investigations
- Provide documentation expertise for corrective action processes
Educational Qualification
Candidates should possess:
- A university degree in Life Sciences
- OR
- Relevant professional experience in a related field
Experience Required
- 2–3 years of label creation experience in:
- Life Sciences
- Medical Devices
- In Vitro Diagnostics (IVD)
Required Skills & Competencies
- Excellent English communication, writing, and editing skills
- Familiarity with:
- Adobe InDesign
- Adobe Illustrator
- Visual and multimedia documentation tools
- Ability to manage multiple documentation projects in a fast-paced global environment
- Understanding of EU IVDR documentation requirements
- Strong attention to detail and documentation accuracy
- Good collaboration and communication skills
- Ability to work independently and within cross-functional teams
- Interest in understanding complex scientific products and systems
Preferred Skills
- Multilingual proficiency in languages such as:
- Swedish
- German
- French
- Spanish
- Experience with EU MDR documentation requirements
- Strong cross-cultural communication abilities
- Continuous improvement mindset and technical curiosity
Preferred Industry Background
Candidates with experience in the following industries will be preferred:
- Medical Devices
- In Vitro Diagnostics (IVD)
- Life Sciences
- Regulatory Documentation
- Scientific Product Labeling
