GMP Technical Writer – Pharma SOPs & Docs

A prominent pharmaceutical organization in St. Louis is seeking a detail-oriented Technical Documentation Writer to support documentation initiatives within a regulated environment. The ideal candidate will have 1–3 years of technical writing experience and strong GMP knowledge. Key responsibilities include authoring SOPs and ensuring compliance with regulatory standards. This position is onsite and offers a 6-month contract with a strong likelihood of conversion to full-time employment. #J-18808-Ljbffr