The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role The Quality Engineer provides support to Quality and Operations on all aspects of the manufacturing process. The position will work to resolve quality issues by ensuring adequate root cause investigations conducted and verifying effectiveness of CAPAs implemented. The position will utilize key Quality Engineering principles, tools, and practices to develop and optimize process controls and quality system processes and identify opportunities to improve quality and cost that are aligned with the overall business goals and QuidelOrtho's Quality Policy. The position will assess risk and will drive quality related decisions. This role is located in Athens, Ohio. The Responsibilities Partner with operations to evaluate and address quality events including nonconformances, product dispositions, customer complaints, root cause investigations, and implement appropriate corrections and/or corrective actions based on risk level. Analyze and monitor key quality metrics and develop action plans to address unfavorable trends. Promote continuous improvement activities by seeking out opportunities to optimize processes and systems to reduce and control variation. Support product and process root cause investigations by collaborating with product support, engineering, and operations. Support and participate in inspection readiness activities by applying working knowledge of ISO13485 and 21CFR Part 820 regulations. Conduct product risk assessments and manage Product Risk Files (i.e. FMEA's). Support change control process. Collaborate with R&D on design transfer activities / plans, that may include, but are not limited to the development of raw material specifications, process controls, and validation. Utilize quality engineering tools such as performing design of experiments, gage R&R, and process capability assessments. Performs other work-related duties as assigned. The Individual Required: B.S. Degree in Chemistry, Biochemistry, Biology, Engineering, or a related discipline. Advanced Microsoft Office (Word, Excel, PowerPoint, etc.) and other statistical software tools (e.g. MiniTab). Experience with establishing sample plans, quality test plans, and summarizing / reporting data analysis, is required. Clearly and effectively documents, communicates, and presents technical information. Works effectively independently as well with a cross-functional team across Operations, Product Support, Compliance, Regulatory, and Suppliers. Demonstrates a high degree of accuracy and attention to details. Strong organization and time management skills. Analytical and problem-solving skills with an ability to use scientific knowledge and statistical methods to identify and resolve issues. Preferred: 1-3 years of experience in Quality in a highly regulated manufacturing environment (Diagnostics, Medical Device, Pharmaceutical, or Consumer). Knowledge of current and applicable GMP regulations including ISO13485 and 21 CFR Part 820. The Key Working Rel