Job Summary Under general supervision, responsible for aligning product labeling content with state and federal regulations. Job Description MAJOR RESPONSIBILITIES: - Review, verify and complete packaging submissions to authorize label related content based on regulations and product claims. Evaluate supporting documentation for relevant regulatory authorities. - Experience with writing and modifying procedures. - Research changes with regulations and review requirements for devices and OTC drugs with stakeholders. - Inform divisions on requirements and content using documentation, market knowledge, and assessment of risk. Influence change to improve processes and eliminate waste. - Identify and execute opportunities for improvement through the simple kaizen process. - Participate in the CTIQ team/Cross departmental team process improvement program. - Conduct internal audits (files, processes, databases, etc.) and maintain department databases, logs and files. - Train and mentor new em...