Quality Engineer III

Responsible for identifying and implementing continuous improvements to improve product performance and complaint processes. Your Responsibilities Will Include: Bachelors Degree Minimum of 3 years of related experience Knowledgeable in Quality System Regulations, Medical Device Regulation, and ISO13485 Quality Standards. Experience in Medical Device industry Familiarity with Post Market requirements and IT systems Demonstrated effective change leadership and results-oriented focus Demonstrated problem-solving & data analysis capabilities Proficient with Microsoft Office tools including Word, Excel, PowerPoint, and Outlook. Strong business acumen and communication skills, with the ability to quickly establish impact and consequences Ability to collaborate and influence across multiple, cross-functional teams Strong ability to successfully multi-task and adaptability Demonstrated experience managing and leading multiple projects covering diverse engineering (i.e. Software, Hardware, Labeling) disciplines and functions. Knowledge of analytical techniques, problem solving, continuous improvement programs, and statistical analysis Self-starter with the ability to identify improvement opportunities. Comfort speaking to groups of individuals including divisional senior leaders. Presentation skills that comfortably and concisely translate performance and issues to peer and senior management audiences. Some potential future people leadership roles