Life Sciences Job at Cepheid
Looking for a high-growth Life Sciences Job in a global biotech company? Here’s your chance to join Cepheid Careers as a Technical Writer in Bengaluru. This is a premium opportunity for life science graduates to work on cutting-edge molecular diagnostics, gain global exposure, and build a career in scientific documentation within the healthcare industry.
Company Overview
Cepheid, part of Danaher’s global network of life sciences companies, is a leader in molecular diagnostics. The company focuses on delivering fast, accurate diagnostic solutions that address complex healthcare challenges worldwide.
Driven by innovation and the Danaher Business System, Cepheid fosters a culture of continuous improvement, collaboration, and impact-driven work. Its flagship technologies, including the GeneXpert® system, play a crucial role in advancing clinical diagnostics and improving patient outcomes globally.
Job Details:
- Job Title: Associate Technical Writer
- Company: Cepheid (a Danaher Corporation company)
- Location: Bengaluru, Karnataka, India
- Job Type: Full-Time | On-site
Job Overview
The Associate Technical Writer is responsible for developing, reviewing, and publishing regulatory-compliant documentation for Cepheid’s diagnostic products, particularly the GeneXpert instrument systems. The role involves collaboration with cross-functional teams to ensure technical accuracy, clarity, and compliance in all documentation.
Key Responsibilities
Documentation Development
- Creates and maintains technical documentation such as:
- Instructions for Use (IFUs)
- Product Manuals
- Getting Started Guides
- Service Manuals
- Ensures all documentation meets regulatory compliance standards.
Content Management & Review
- Reviews and updates documentation to reflect product changes and stakeholder feedback.
- Documents product functionalities across Cepheid product lines.
- Ensures consistency, clarity, and usability of technical content.
Cross-Functional Collaboration
- Works closely with Regulatory Affairs, Clinical, Product Management, and Engineering teams.
- Ensures documentation aligns with user requirements and technical specifications in a regulated environment.
Global Content Development
- Develops localization-ready content suitable for global distribution.
- Maintains high-quality standards for international audiences.
Qualifications
Essential Requirements
- Bachelor’s or Master’s degree in Life Sciences, Biomedical Engineering, or related fields.
- Minimum 2+ years of experience in technical writing (software or hardware environment).
- Proficiency in authoring tools such as:
- Vasont
- MadCap Flare
- Adobe FrameMaker
- Strong understanding of document management and version control systems.
- Excellent written and interpersonal communication skills.
- Ability to quickly learn molecular diagnostic technologies such as PCR and clinical lab workflows.
Preferred Qualifications
- Experience working in regulated environments (e.g., medical devices or diagnostics).
- Knowledge of regulatory standards, including:
- FDA 21 CFR Part 820 / Part 11
- ISO 14971
- GAMP 5
- Familiarity with corporate style guides and compliance-driven documentation practices.
Work Environment & Benefits
- On-site role at Danaher India Development Center (IDC), Bengaluru
- Collaborative and innovation-driven culture
- Competitive benefits including healthcare and paid time off
- Opportunities for career growth within a global organization
Role Impact
The Associate Technical Writer plays a critical role in ensuring that Cepheid’s diagnostic solutions are supported by accurate, compliant, and user-friendly documentation, enabling healthcare professionals worldwide to effectively use life-saving technologies.
