Ajilon Consulting is an international IT consulting firm with offices worldwide. We have over 6,000 consultants in over 80 cities in the United States, as well as in Canada, the United Kingdom and Australia. If you're looking for a company that takes pride in its people, rewards loyalty, has a solid reputation and a passionate commitment to a global vision -- consider a career at Ajilon
Experience: The senior writer works with internal staff to produce a variety of team documents that may include presentations, requirements, white papers, and so on.
The ability to work with a variety of subject matter experts to produce cohesive documents is required. Experience in Visio, Powerpoint, and various desktop publishing tools is required. Must have demonstrated experience using Adobe Framemaker.
Experience creating documentation for the IT/Software domain is preferred. Poise working with Senior Staff will also be required for this position.
Key Responsibilities
Researches, writes, and edits a variety of technical documents for FDA-regulated medical devices (primarily software). Manages technical writing schedules for multiple, concurrent deliverables.
You will work collaboratively with other team members to improve the ease of use and functionality of new products globally. You will use your proven ability to apply tools and processes to resolve complex communication challenges in creative and effective ways.
Required Background
Familiarity with the medical electronics industry and FDA, GMP, and ISO regulatory compliance is a plus. An excellent knowledge of the product development process is a plus, as well as strong computer skills such as FrameMaker, MSWord, graphics programs, and Excel. The ideal candidate must possess excellent written, verbal and interpersonal communication skills as well as be collaborative, inquisitive, analytical, and decisive.
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