Iatric Manufacturing Solutions produces FDA-regulated wet wipes in controlled manufacturing environments where temperature and humidity are carefully managed to minimize environmental influences on our products and ensure comfortable working conditions for our team. What You’ll Do As a Quality Engineer II , you will: Develop and execute validation protocols (IQ/OQ/PQ) for equipment, sanitation, facilities, software, and processes. Collaborate with customers on equipment and process validations. Serve as the database administrator for Infinity QS (Statistical Process Control) software. Provide statistical analysis support for manufacturing, new product development, trials, and validations. Develop SOPs related to validation and risk management. Monitor and prepare Key Performance Indicators (KPIs) for major customers. Lead Corrective Action/Preventative Action (CAPA) activities and facilitate root cause investigations. Train associates on quality topics such as SPC and CAPA. Drive continuous improvement initiatives with internal teams and external partners.