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Clinical Diagnostic Senior Technical Writer

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Job duties include but are not limited to:
• Work with R&D, Customer Solutions, Marketing, and Regulatory to plan, write, and edit clinical/diagnostic technical documentation for scientific audiences including clinicians, physicians, and patients.
• Collect data by interviewing specialists, researching written material, attending training and demonstrations, using products, and observing users.
• Work efficiently and accurately in content management systems, adhering to best practices and departmental standards for terminology, content management, and reuse.
• Take photographs to illustrate the documentation and work with an illustrator to convert them to technical drawings.
• Release finished documentation to Document Control (SAP PLM), and maintain organized records of all materials, drafts, and previous versions.
• Coordinate one or more functional areas, such as localization management.
• Quickly learn and apply new tools, processes, and standards. Demonstrate adaptability and forward thinking in the face of technological or organizational change.
• Propose technical improvements to authoring tools and work with technical leads to evaluate and implement.
• Initiate and drive projects to improve customer experience, efficiency, and sensible cost avoidance. Support similar initiatives driven by others on the team.
• Train and mentor new writers. Help build a strong training infrastructure so that writers across the company benefit from new discoveries and developments.
• Occasional travel required.

Education and Experience:
Bachelor's Degree or equivalent. Scientific knowledge a plus.
Five to eight years of experience as a technical writer in a regulated clinical/diagnostic environment (software, hardware, biotech).

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