Responsibilities include but not limited to:In collaboration with process engineering team:Develop and optimize processes for manufacturing medical devices.Conduct characterization studies.Document study results in technical documents and work instructions.Perform data analysis.Assist with the startup of new equipment/product by developing process parameters. Participates in data analysis to optimize the process.Maintain process databases and document process changes. Troubleshoot issues related to process, machine and materials Adhere to safety protocols to ensure a safe work environment. Follow Good Manufacturing Practices (GMPs).Experience & Skills:High school diploma required.Associate or technical certification preferred.Minimum of 5 years of experience with Nitinol medical devices and/or complex catheter development required.Strong written and verbal communication skills.Proficient in math for data analysis.Microsoft Office skills required.Effective organizational & time management skills and attention to detail.Strong problem-solving skills focused on root cause analysis.Experience with tool machining and/or chemical processing a plus. recblid ibmilr4h71ocmje3kjvbxvta1l4kne