Sr.DeviceEngineer

**Use Your Power for Purpose** This role has primary responsibility for confirmation that medical devices and drug/device combination products meet their intended function. This includes development of data through engineering studies that informs new product development as well as test reports that support product submissions. The candidate will work within a team environment to solve problems and utilize best engineering practices and techniques for root cause and statistical analysis. This work entails defining test methods, developing protocols, performing data analysis, and writing reports in compliance with corporate procedures. **What You Will Achieve** In this role, you will: * Partner with Systems engineers in defining product requirements such that they are verifiable * Development of test fixtures, test methods, and performance of Test Method Validation activities * Coordinate with internal and external partners and suppliers to procure test samples and manage conditioning and accelerated aging studies * Ensure integrity and compliance of data according to Standard Operating Procedures * Develop Verification Plans including test strategy * Utilize technical writing and statistical data analysis skills to write protocols and reports * As necessary, conduct root cause analysis and derive recommendations based on analysis of data * Translate inspections and tests methods into component and product specifications * Potential for Project Team lead responsibilities including MS Project schedule creation/maintenance, device team meetings, and overall team management. **Here Is What You Need**(Minimum Requirements) * Applicant must have a bachelor's degree with at least 2 years of experience; OR a master's degree with 0+ years of experience; OR an associate's degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant experience **Bonus Points If You Have**(Preferred Requirements) * Experience in the pharmaceutical or biote