Technical

Overview This position is NonExempt. Hours over 40 will be paid at Time and a Half. Writes a variety of technical articles, reports, brochures, and/or manuals for documentation for a wide range of uses. May be responsible for coordinating the display of graphics and the production of the document. Familiar with variety of the field's concepts, practices and procedures. Relies on experience and judgment to plan and accomplish goals. May lead and direct the work of others. A wide degree of creativity and latitude is expected. May require a bachelor's degree or 4-6 years experience. Notes from Manager Technical writer to reformat our Risk Management Plan (RMP) documentation. Existing RMP documents are a critical part of the company's product definition. These documents need to be reformatted to include updated definitions and references. The senior technical writer should preferably have experience working with FDA - or other regulated industry – practices and ISO systems. Qualifications Proficient in Microsoft Word: advanced editing, commenting, routing, formatting Proficient in Microsoft Excel: editing, formatting Prior experience Technical Writing in the medical device industry needed with particular emphasis in writing SOPs and document changes. #J-18808-Ljbffr Olsa Resources