At Cepheid, one of Danaher’s operating companies, our work saves lives by innovating fast, accurate molecular diagnostic systems and tests
Job Summary
At Cepheid, one of Danaher’s operating companies, our work saves lives by innovating fast, accurate molecular diagnostic systems and tests.
The Lead Technical Writer will create and manage regulatory-compliant documentation, collaborating with cross-functional teams to ensure technical accuracy and user needs are met.
Cepheid offers comprehensive, competitive benefits that contribute to life beyond the job and fosters an environment of career growth and development.
Matching Summary
At Cepheid, one of Danaher’s operating companies, our work saves lives by innovating fast, accurate molecular diagnostic systems and tests.
Skills & Requirements
Must-have
regulatory-compliant documentation development
technical writing in regulated environment
authoring tools expertise
graphics and video editing skills
collaboration with regulatory and clinical teams
Nice-to-have
managing translation workflows
leading small projects and mentoring
knowledge of FDA and ISO regulations
integrating AI-driven workflows
cloud capabilities for content lifecycle
Key Requirements
Bachelor’s or master’s degree in relevant field
5+ years technical writing or software validation experience
2+ years project management in regulated environment
experience with FDA, EU MDR/IVDR, ISO 13485 standards
proficiency in professional authoring and editing tools