GMP Lead & Manufacturing Specialist

A medical device company in Pennsylvania is seeking a GMP Associate III. This role ensures compliance with GMP, FDA, and ISO 13485 standards, leading safety practices and quality checks. Candidates should have 2-4 years of experience in a GMP-regulated environment and a strong ability to troubleshoot equipment issues. Responsibilities include training team members and driving continuous improvement through lean initiatives. A high school diploma is required, and technical certification is preferred. #J-18808-Ljbffr