Pharma GMP Quality Documentation Specialist

A pharmaceutical company in Indiana is seeking a Quality Assurance Technical Writer to manage documentations during the startup phases of a new GMP site. This role involves developing and maintaining SOPs and reports, collaborating with subject matter experts for accuracy, and ensuring compliance with standards. Ideal candidates will have 3-5 years of pharma GMP writing experience and familiarity with document management tools like Veeva Quality Docs. #J-18808-Ljbffr