Associate Technical Writer
Danaher View all jobs
- Bangalore, Karnataka
- Permanent
- Full-time
- Work as an individual contributor and develop, review, update, and publish regulatory-compliant documentation, including IFUs, Product Manuals, Getting Started Guides, and Service Manuals.
- Document product functionalities and manage documentation reviews to verify that technical information for all Cepheid product lines.
- Collaborate with Regulatory Affairs, Clinical, product management, and engineering teams to ensure documentation meets user needs and technical accuracy within a regulated environment.
- Create high-quality, localization-ready content designed for seamless adaptation across global regions.
- Bachelor’s or master’s degree in Computer Science, Technical Communication, English, Life Sciences, or a related Engineering field (e.g., Biomedical).
- 2+ years of professional technical writing experience in a software or hardware environment.
- Mastery of professional authoring tools (e.g., Vasont, MadCap Flare, FrameMaker) and a strong working knowledge of document management and version control systems.
- Excellent interpersonal and writing skills, with self-motivation to quickly learn new molecular diagnostic technologies, such as PCR and clinical lab workflows.
- Working knowledge of key regulations, including FDA 21 CFR Part 820/Part 11, ISO 14971 (Risk Management), and GAMP 5, with the ability to maintain strict adherence to corporate style guides.
- Experience in a regulated environment such as a medical domain, is a plus.