On-Site Contract Technical Writer — FDA-Regulated

A leading life sciences consulting firm is seeking an experienced Technical Writer to join their team in Kenosha. The ideal candidate will have at least five years of experience in FDA-regulated environments, authoring compliant documentation such as SOPs and protocols. This role requires strong interpersonal skills and attention to detail. Candidates must be able to work on-site and effectively interact with subject-matter experts to create high-quality documentation. An excellent opportunity for professionals looking to make a difference in patient care. #J-18808-Ljbffr