Principal Quality Engineer

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

Principal Quality Engineer Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Principal Quality Engineer will be the liaison to cross function departments (e.g. Research and Development, Operations and etc.) with respect to investigations and/or results of investigations related to complaints. The lead is responsible for providing recommendations on product improvements as well as serve as the technical lead on large CAPA investigations where the incumbent will develop test methods to identify root/potential causes of complaints. Must be able to analyze data and assist in interpreting the data. Develop and implement investigation process improvements.

Responsible for implementing and maintaining the effectiveness of the quality system. Proactively utilize technical depth to understand complaints and works to improve products/process to better meet customer needs with reduced issues. Provides guidance with respect to applicable complaint investigation processes, and ensures compliance with regulations with respect to investigations. Sets global standards for specifications and drawings that properly identify and highlight critical quality attributes. Capture complex technical requirements in policies, design plans, investigations. Translates business strategy into meaningful objectives and day-to-day activities required to accomplish them. Anticipates future direction and adjusts current processes accordingly. Effectively communicates directional changes and creates support for changes. Be the technical lead for complaint investigations, and be liaison to other functions, such as R&D, Operations, and other Quality functions. Ensure investigation results are disseminated to the relevant SMEs appropriately. Structures studies and integrates cross-disciplinary and cross-functional issues to arrive at optimal cause of action, e.g. investigates process to meet increasing regulatory requirements while maintaining manufacturing/system construction efficiency. Follows through on project goals; contributes willingly and incorporates the ideas of others; shares resources, knowledge and accountability to benefit the objectives of the business, e.g. participates in team meetings; serves either as functional subject matter expert or independent technical expert in management reviews. Strong project management skills and able to multi-task and set priorities to meet overall business objectives.

BS in Math, Science, or Engineering disciplines preferred, or equivalent combination of education and work experience will be considered Minimum 5 years of Quality experience in a FDA/ISO regulated environment. Preferred