In this role, you will be responsible for:
61 Managing the revision of global technical documentation for hardware, software, and reagent products.
61 Performing research, working with prototypes, and collaborating with subject matter experts to write end-user documentation, including instrument instructions for use manuals, system guides, quick start guides, and field service manuals.
61 Driving project scheduling and planning to ensure on-time delivery.
61 Overseeing the correct, complete, and compliant execution of product requirements in all deliverables and working with the appropriate subject matter experts to resolve problems and exceptions.
61 Demonstrating proficiency through the content development process to meet company strategies and business objectives.

The required qualifications for the job include:
61 Bachelor's degree.
61 Fluent in the English language.
61 Minimum 2 years of direct work experience as a technical writer, preferably in medical diagnostics, scientific, or a medical device manufacturing company.
It would be a plus if you also possess previous experience in:
61 The Life Sciences/Medical Device industry.
61 Structured FrameMaker.
61 Managing translation projects and content management systems.