Job Title: Senior Quality Assurance Engineer Location: Redmond, WA Hours/Schedule: 3:30 PM-2:00 AM Monday - Thursday, flex Friday as needed Compensation: $46.66- $53.00 Type: Contract Overview Global Medical Device company looking to hire experienced Quality Assurance Engineer to join their growing team. This is not an IT role! Responsibilities + Work closely with Operations and the business functions to ensure quality performance of product and processes. + Non-Conformances + Collaborate with Internal cross-functional and Supplier teams to address top quality issues. + Own identified internal and supplier-driven Non-Conformances (NC) and Corrective Action Preventative Action records (CAPA), managing the timely processing and closure of NC and CAPA records within the electronic management system, Trackwise. + Support execution and analysis of manufacturing related complaint investigations + Investigate and disposition internal non-conforming product within MRB, issuing NCs as appropriate. + Supplier Activities + Communicate & collaborate with suppliers regarding non-conformances, escalating Supplier Corrective Action Requests (SCAR) as required. + Execute and manage Supplier Initiated Change Requests (SICRs) received from suppliers, engaging with cross-function teams for assessment and approval + Collaborate with appropriate stakeholders to identify and execute opportunities for supplier part certification. + Process Improvements/Validation + Engage in the development and improvement of the internal manufacturing and distribution processes for existing products. + Perform critical assessments and qualifications of internal and supplier-proposed change management activities, including Production Part Approval Process (PPAP) activities for supplier changes. + Participate in and potentially lead the creation and/or review of new or modified procedures. + Support the development and review of process and equipment validation/qualification and MSA of internal processes. + Maintain KPIs for monitoring of process and/or product quality, perform analysis, and interpret trends, identifying and activating on appropriate actions as necessary. + Perform other related duties as assigned. Requirements + Bachelor’s degree in an Engineering/Science/technical field or a related field + 1-3 years of experience in quality assurance + Medical Device experience is highly preferred Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan. Ref: #558-Scientific System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.