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Create and edit operational, instructional, and maintenance/test procedures for paper, digital, or web-based publication.
Convert existing documentation into data collection plans, for use in the digital record system.
Communicate with various users and technical staff to gather data for documentation.
Document Engineering processes and specifications. Recommend format, regarding technical and customer requirements.
Produce documentation that conforms to the company documentation and quality assurance standards.
Interface with process owner(s) to ensure documentation matches current best practices.
Release and maintain documents in PLM system.
Associate degree or equivalent work experience as a technical writer or generating documentation for medical devices.
Experience working in a highly regulated industry and following mandatory processes (preferably in the medical device industry).
Excellent written and verbal communication skills.
Good organizational skills (task tracking and reporting).
Strong experience with Microsoft Office (including redlining function), and Adobe Acrobat.
Experience with document control software (ideally MyWorkshop PLM) is desirable
Legal authorization towork in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.
Sitting
Standing
Lifting <25 pounds
Computer typing
Computer monitor
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