GMP QA Technical Writer - Startup Site, Onsite

A leading pharmaceutical company is seeking a detail-oriented Quality Assurance Technical Writer for their new GMP manufacturing site in Lebanon, IN. This position involves developing and managing quality documentation, ensuring compliance with regulatory standards. The ideal candidate will have a Bachelor's degree and 3–5 years of experience in technical writing within a GMP environment. Strong communication skills and familiarity with electronic document systems like Veeva Quality Docs are essential. This is an onsite role offering an exciting opportunity to contribute to a startup environment. #J-18808-Ljbffr