Senior Technical Writer – Medical Device & FDA Docs

A technical writing firm in Princeton seeks a Senior Technical Writer to reformat Risk Management Plan (RMP) documentation crucial for product definition. The ideal candidate will possess experience in the medical device industry, particularly in writing standard operating procedures (SOPs). Proficiency in Microsoft Word and Excel is essential. This role demands creativity and attention to detail, as well as familiarity with FDA regulations. Competitive compensation and a collaborative work environment are offered.
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