Engineer II, R&D, Packaging Test Lab

Imagine how your ideas and expertise can change a patient’s life. Our Global Operations & Quality team plays a central part in ensuring our products are delivered to patients with cardiovascular disease. You’ll partner cross-functionally with manufacturing operations and sales teams, delivering thoughtful solutions to complex challenges all while developing your knowledge of the medical device industry. Whether your work includes strategic inventory planning, labeling, warehouse management, material handling, or any of our other supply chain opportunities, you will be making a meaningful contribution to our team and to patients all over the world.  The R&D Packaging Test Lab Engineer II applies knowledge of technical principles and Edward’s systems/procedures to optimize product development. How you’ll make an impact: Design, execute, and document package testing and validation activities to support product development, manufacturing, supplier qualification, process changes, and regulatory requirements. Develop, validate, and continuously improve test methods, protocols, work instructions, fixtures, and laboratory processes for sterile and non-sterile medical device packaging systems. Analyze test data using statistical and engineering principles; identify trends, investigate anomalies, and provide technical recommendations to internal customers and project teams. Lead or support equipment qualification activities (IQ/OQ/PQ), method validations, and laboratory investigations to ensure compliance with quality system and regulatory requirements. Drive laboratory process improvement and automation initiatives, including workflow optimization, digital data collection, data analytics, test scheduling, and implementation of laboratory technologies that improve efficiency, quality, and throughput. Support management of external testing suppliers by defining technical requirements, reviewing supplier test reports, and ensuring quality and service expectations are met. Provide technical direction and day-to-day guidance to technicians, including test execution, troubleshooting, training, workload coordination, and continuous skills development. Other duties assigned by Leadership. What you’ll need (Required): Bachelor's Degree in Engineering or Scientific field with 2 years experience or Master's Degree or equivalent in Engineering or Scientific field with internship, senior projects, or thesis in Engineering or Scientific field including either industry or industry/education. What else we look for (Preferred): Experience with laboratory testing environments, engineering test methods, validation activities, troubleshooting, maintenance coordination, calibration oversight or medical device product testing. Knowledge of statistical methods and data analysis tools (e.g., Minitab, Excel, Power BI, or similar platforms). Experience improving business processes through automation, digital transformation, workflow optimization, data analytics, or software-enabled solutions. Familiarity with regulated environments and quality systems, including design controls, validation principles, change control, CAPA, and good documentation practices. Strong technical writing skills with the ability to prepare protocols, reports, work instructions, requirement specifications, risk assessments, engineering records, design control deliverables and validation documentation. Ability to manage multiple projects simultaneously while balancing technical, quality, regulatory, and business requirements. Strong problem-solving, root cause investigation, and critical thinking skills. Ability to collaborate effectively with cross-functional stakeholders, external suppliers, and project teams. Experience with medical device packaging, package validation, transportation testing, environmental conditioning, sterilization validation support, or related laboratory activities is preferred. Experience with automation, scripting, AI-enabled tools,