Senior QA & Documentation Systems Specialist

A pharmaceutical company in North Carolina seeks a Sr. Quality Specialist I, Documentation Systems. This role involves conducting quality compliance activities per GxP regulations and managing documentation practices. The ideal candidate will have a bachelor's degree, 6+ years in quality systems, and strong problem-solving abilities. Responsibilities include product complaint investigations, SOP authoring, and supporting regulatory submissions. This position is a critical role in maintaining quality standards and improving patient care. #J-18808-Ljbffr