GMP SOP Writer & Documentation Lead

A dynamic technology company in Wayzata is seeking an individual with 5-8 years of experience in a GMP laboratory to write and revise standard operating procedures. The candidate will collaborate with cross-functional teams, manage project timelines, and utilize tools like Veeva EDMS and SAP. Strong technical writing skills and the ability to influence without authority are key to success in this role, alongside a detail-oriented approach to document management. #J-18808-Ljbffr