We are the people who give possibilities purposeBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. 

Job DescriptionResponsibilities:Provide quality engineering support for manufacturing processes to ensure compliance with FDA regulations, ISO standards, GMP requirements, and company quality system procedures.Lead and support investigations related to nonconformances, deviations, customer complaints, out-of-specification results, audit findings, and other quality events to determine root cause and implement effective corrective and preventive actions CAPA.Evaluate manufacturing processes and quality data to identify trends, improve process capability, reduce defects, and drive continuous improvement initiatives.Develop, review, and approve quality documentation, including procedures, work instructions, specifications, protocols, reports, risk assessments, and validation documentation.Support product and process validation activities, including IQ/OQ/PQ, process validation, cleaning validation, software validation, and test method validation, as applicable.Participate in change control activities by assessing the quality and regulatory impact of proposed changes to products, processes, materials, equipment, and systems.Utilize quality engineering tools and methodologies, including statistical analysis, process capability studies, root cause analysis, Failure Mode and Effects Analysis FMEA, and risk management techniques.Analyze quality metrics and performance indicators, including scrap, yield, nonconformances, complaint trends, and process performance data, and recommend improv
