QA - IDM Device Complaints

Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Job Description: Support the Product Complaint Handling and Medical Device Reporting Processes. This role is designed for an individual who is curious, embraces new digital tools and ways of working, and helps drive practical change across complaint reporting, trending, and stakeholder support. Specific functions, duties, or tasks: - Author/review/approve GMP documents including technical reports, deviations, change controls, inspection procedures, process level procedure, and work instructions - Lead authoring and management of deliverables to support Global Patient Safety and device safety case reporting - Author regulatory responses and re...