GxP Technical Writer & Process Documentation Lead

A leading pharmaceutical organization in Clayton, NC is seeking a Technical Writer to manage documentation aligned with GxP standards. Responsibilities include developing Standard Operating Procedures (SOPs) and training materials while collaborating across functions to support process improvement. The ideal candidate has over 3 years of experience in pharmaceutical technical writing, excels in project management, and possesses proficiency in tools like MS Word and Visio. This position offers an opportunity to contribute to operational excellence in a regulated environment. #J-18808-Ljbffr