Kforce is seeking to hire two experienced Technical Writers with Pharma and/or Medical Device documentation experience for contracting needs in the West Michigan job market. These positions focus on: * Researches, prepares, and edits complex technical documents related to Quality Systems * Supports changes to Quality System documents as a result of a corporate validation project * Remediates Quality System documents in response to an FDA finding * Also involves meeting with process owners, write change descriptions, revise procedures and coordinates with Training Department / Process Owners Qualifications: * 5 years of Technical Writing experience are required * Pharmaceutical and/or Medical Device experience to include procedure writing experience, document control experience (maintaining linkages, controlled release, and compliance knowledge) is required * Candidates should also have critical thinking skills, pay attention to detail, and have the ability to facilitate discussions / troubleshoot with process owners