GMP Quality Assurance Technical Writer (Contract)

A leading provider in health compliance solutions is seeking a Quality Assurance Technical Writer for an 18-month contract in Lebanon, Indiana. The role involves developing and maintaining technical documentation, ensuring accuracy while collaborating with subject matter experts. Candidates should have 3-5 years of pharma GMP technical writing experience and familiarity with Veeva Quality Docs. This position provides an opportunity to contribute to the startup phases of a new GMP site and ensure compliance with industry standards. #J-18808-Ljbffr