Regulatory Labeling Specialist

Job Summary Under general supervision, responsible for aligning product labeling content with state and federal regulations. 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 employees, divisional QA's and product managers on regulatory product structure, regulatory labeling requirements, and Medline labeling procedure(s). Education and Experience Bachelor’s Degree in Science or related field. At least 2 years of experience in Quality or Regulatory Affairs for a regulated industry. Knowledge / Skills / Abilities Knowledge and understanding of FDA product codes and product class structure, Quality Management Systems and Good Manufacturing Practices, or willingness to learn through training and independent research. Excellent communication and relationship building skills, project management, critical thinking and problem solving abilities to deliver results and meet deadlines. Preferred Job Requirements At least 2 years of experience in a product labeling-related role for a regulated industry. Experience evaluating regulatory risk. Experience in project management using critical thinking and problem-solving abilities to deliver results. Experience in evaluation of information to determine compliance with standards, laws, and regulations. Compensation The anticipated salary range for this position: $79,000.00 - $119,000.00 Annual. The actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Benefits Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. EEO Statement Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws. #J-18808-Ljbffr