Technical Writer Jobs | Cepheid is Hiring | Apply Now
Looking for high-growth technical writer jobs in the life sciences industry? The latest Cepheid career opportunity in Bengaluru offers a unique chance for candidates with a background in biotechnology, diagnostics, or regulatory documentation. If you’re aiming to build a strong profile in life sciences jobs, this role lets you work on cutting-edge molecular diagnostic technologies like PCR and GeneXpert systems.
- Job Title: Technical Writer
- Location: Bengaluru East, Karnataka, India
About the Company
Cepheid is a globally recognized biotechnology company focused on molecular diagnostics and improving healthcare outcomes. As part of Danaher, Cepheid leverages advanced technologies to deliver fast and accurate diagnostic solutions. The company is known for its GeneXpert systems, widely used in clinical and laboratory settings. Cepheid operates at the intersection of life sciences, diagnostics, and innovation. With a strong global presence, it continues to lead advancements in PCR-based testing. The organization promotes continuous improvement and impactful scientific contributions.
Key Responsibilities
- Perform duties as an individual contributor and team member with 100% hands-on work to 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 Xpert tests and GeneXpert systems.
- Collaborate with Regulatory Affairs and Clinical 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.
- Build deep knowledge of company processes, molecular diagnostic technologies (like PCR), and customer needs to drive continuous quality improvements.
Qualifications
- Bachelor’s or master’s degree in Life Sciences, or a related Engineering field (e.g., Biomedical).
- 3–5 years of professional technical writing or software validation testing experience in a strictly regulated environment such as Medical Devices, IVD, or Biotechnology.
Preferred Skills & Experience
- Experience in creating regulatory-compliant documentation (IFUs, user manuals, QRIs) aligned with FDA, EU MDR/IVDR, and ISO 13485 standards
- Proficiency in authoring tools such as Vasont, MadCap Flare, and FrameMaker, along with document management and version control systems
- Strong writing and interpersonal skills with the ability to quickly learn molecular diagnostics (e.g., PCR, clinical workflows)
- Ability to manage translation workflows for global markets and handle small project leadership responsibilities
- Experience in training or mentoring team members to ensure documentation quality and consistency
- Working knowledge of FDA 21 CFR Part 820/Part 11, ISO 14971, and GAMP 5 regulations
- Ability to adhere to corporate style guides and regulatory documentation standards
- Experience integrating AI-driven workflows and cloud-based tools to optimize content lifecycle management
- Capability to manage multiple documentation projects while ensuring quality and compliance
- Focus on delivering high-quality user documentation to support customer satisfaction
If you’re serious about landing top technical writer jobs, this Cepheid career is a game-changing opportunity. With exposure to global diagnostics systems and regulatory environments, this role can significantly boost your profile in life sciences jobs.
