Life Science Job at Thermo Fisher Scientific
Are you searching for a rewarding Life Science Job that combines scientific expertise with communication skills? Here’s an exciting chance to join one of the world’s leading scientific organizations through Thermo Fisher Scientific Careers. This latest Technical Writer Job in Bangalore is ideal for professionals passionate about life sciences, medical devices, and scientific documentation. If you are looking for an excellent opportunity for life science graduates to work in a global research-driven company, this opening could be your next career breakthrough.
About Thermo Fisher Scientific
Thermo Fisher Scientific is one of the world’s leading scientific research and healthcare companies, serving customers in pharmaceuticals, biotechnology, healthcare, diagnostics, food safety, and academic research. Through innovative technologies and advanced scientific solutions, Thermo Fisher Scientific Careers provide professionals with opportunities to contribute to cutting-edge research and healthcare advancements globally. The company is widely recognized for offering strong career growth, inclusive work culture, and excellent opportunities for scientific professionals seeking a successful Life Science Job.
Job Details
- Job Title: Technical Writer – Manuals
- Company: Thermo Fisher Scientific
- Location: Bangalore
- Job ID: R-01351899
- Job Type: Full-time
- Category: Research & Development
- Work Mode: Fully Onsite
- Work Schedule: Standard (Monday–Friday)
- Environmental Conditions: Office
Job Description
As part of the Thermo Fisher Scientific team, employees contribute to impactful work that supports a healthier, cleaner, and safer world. The organization provides opportunities to work on solutions addressing major global challenges, including environmental protection, food safety, and healthcare innovation.
Key Responsibilities
- Develop, update, and proofread high-quality:
- Instrument User Manuals
- Software User Manuals
- WebHelp manual packages
- Other technical documentation
- Simplify complex scientific, technical, and regulatory information into clear and user-focused documentation.
- Improve document text, layouts, and images to enhance quality and usability.
- Ensure compliance with:
- QSR
- ISO standards
- Internal quality and regulatory requirements
- Coordinate translation activities with external agencies and internal stakeholders.
- Follow company style guides, templates, and Quality Management Systems (QMS).
- Collaborate with cross-functional teams including:
- Product Development
- Research & Development
- Regulatory Affairs
- Quality Assurance
- Marketing
- Global Operations
- Manage documentation activities within assigned responsibilities.
- Contribute to continuous improvement of documentation standards and processes.
- Support Deviation, CAPA, and complaint investigations through documentation expertise.
Qualifications & Experience
Required Qualifications
- Bachelor’s or Master’s degree in:
- Life Sciences (Biology, Biochemistry, Molecular Biology, etc.)
- Related fields
- Equivalent professional experience may also be considered.
Required Experience
- 3–4 years of technical writing experience in:
- Life Sciences
- Medical Devices
- In Vitro Diagnostics (IVD) industry
Technical Skills
- Excellent English communication, writing, and editing skills
- Understanding of regulated content development and labeling requirements
- Hands-on experience with CMS/CCMS systems
- Experience with DITA/XML structured authoring environments
- Ability to manage multiple projects in regulated global environments
- Experience with translations and simplified English
- Familiarity with EU IVDR documentation requirements
Preferred Skills
- Ability to create compliant and user-friendly documentation for:
- Laboratory technicians
- Clinicians
- Regulatory reviewers
- Multilingual abilities (German, French, Spanish, etc.)
- Experience with reusable content strategies
- Strong cross-cultural communication skills
- High attention to detail and commitment to continuous improvement
- Technical curiosity and ability to understand complex systems
- Ability to work independently and collaboratively
- Experience with EU MDR documentation is an added advantage.
