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. ## **JOB DESCRIPTION:** **Job Title** Quality Engineer **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and 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 of which you dream. - 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 high employer contribution - Tuition reimbursement, the [Freedom 2 Save](https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and [FreeU](https://www.abbott.com/corpnewsroom/strategy-and-strength/college-degree-for-free-its-possible-with-freeu.html) 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 around the world 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 a best place to work for diversity, working mothers, female executives, and scientists. **The Opportunity** This position works out of our Houston, TX location in the Abbott Vascular Division. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for the treatment of vascular disease. THIS IS AN ONSITE DAILY REQUIRED POSITION. What You’ll Work On This position is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within manufacturing and during product manufacturing site transfer activities. MAIN RESPONSIBILITIES • Identify and implement effective process control systems to support the qualification and on-going manufacturing of products in compliance with FDA 21 CFR Part 820/ISO 13485 requirements • Lead implementation of quality assurance processes, process controls, and CAPA systems in alignment with regulatory and internal requirements • Assist in the development and execution of business systems that effectively identify, escalate, and resolve quality issues within a regulated framework • Apply structured problem-solving methodologies (e.g., DMAIC, root cause analysis) to investigate and resolve quality issues • Design and conduct experiments to support process validation, optimization, and continuous improvement • Develop and approve validation documentation including protocols and reports (IQ/OQ/PQ, TMV where applicable) • Lead process control and monitoring of Critical-to-Quality (CTQ) attributes and specifications • Lead and implement continuous improvement initiatives using Lean Manufacturing and Six Sigma methodologies • Lead nonconformance investigations, including NCR, CAPA, and complaint-related analysis, ensuring timely closure and effectiveness verification • Participate as a core team member representing Quality in cross-functional product transfer and sustaining teams • Lead and maintain risk management activities in accordance with ISO 14971, including hazard analysis, risk assessment, and risk control verification • Work with Microbiology and Manufacturing to ensure compliance with environmental monitoring, contamination control, and sterilization requirements where applicable Required Travel: 10-15%. For the first 6-12 months travel could be up to 50% including travel outside of the United States. **Required Education** Bachelors Degree Engineering or Technical Field. **Required Experience** - 2+ years Engineering experience an…