Quality Technician

Duration: 12 Months Contract with possibility of extension Job Description: The Systems Test Role is a Quality Technician who directly supports medical device product development from concept through commercialization by executing tests and assisting with test method development for both new product development and sustaining activities. This role utilizes configurations that closely represent real-world use by healthcare professionals to ensure accurate and meaningful test results. This position works closely with a high-performing, cross-functional sustaining team to ensure the safety, quality, and compliance of launched products while continuously improving their commercial value throughout the product lifecycle. The role is primarily focused on hands-on testing and supporting test development activities to verify and satisfy product requirements. Responsibilities: Support testing efforts to satisfy product requirements for design verification. Execution of testing per documented work instructions. Support Engineers in development and help to facilitate the execution of Design Validation and Verification activities. Perform various tasks to support test lab daily operations, such as lab organization, assisting in assembling equipment and fixturing, stocking lab supplies, and ordering equipment. Assisting in equipment tracking and organization. Hardware and software installation. Perform tasks that assist in identifying, communicating, and resolving quality issues. Document results of testing thoroughly and accurately. Actively promote and participate in a cross-functional teamwork environment. Self-motivated with a passion for solving problems and a bias for action Hands-on approach to work Mechanical aptitude Desire to learn new skills Willingness to perform a wide variety of work tasks Experience using Microsoft Office Preferred qualifications: 2 Year Technical Degree Preferred Previous experience running testing equipment 0-2 years of experience in quality, product development or related medical device / regulated industry experience #J-18808-Ljbffr