Research, plan, outline and write technical documents to support medical imaging products and projects.
Performs Technical Publications administrative duties, such as filing, copying, binding, and archiving, as required and assigned.
Attends planned training on departmental procedures, and on general product principles and operations. Pro-actively solicits training from in-house technical experts (project managers, engineers, applications specialists, etc.) to help with design and development of technical documentation.
Ensures design and production methods and processes are executed in a manner which supports the Quality Policy as well as all ISO Quality System procedures and guidelines.
Other duties as required.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the basic knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Understanding electro-mechanical assembly/dis-assembly processes, user interfaces, and field calibration and alignment procedures
Proficiency with Adobe Frame Maker, Adobe Acrobat and Microsoft Office is required. Familiarity with content management systems (Author-it) is a plus..
Strong Windows based computer literacy and file management abilities specializing in maintaining a digital archive library.
Understanding of MRP's and engineering release standards and processes. Education
- Bachelor's Degree Experience
- 3-5 years related experience writing technical documents for a medical device manufacturing facility a plus Specialized Knowledge
Hologic - 23 months ago
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Hologic corporation is a developer, manufacturer and supplier of diagnostic and medical imaging systems related to women's health. It...