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 114,000 colleagues serve people in more than 160 countries. Job Title Sr. Supplier 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 Opportunity Our location in Scarborough, ME currently has an opportunity for a **Sr. Supplier Quality Engineer** . The **Sr. Supplier Quality Engineer** will partner with supplier & internal customers to identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of supplied material to meet or exceed internal and external requirements. **WHAT YOU’LL DO** + Assist in the development and execution of streamlined business systems which effectively identify and resolve supplier quality issues. + Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving supplier quality issues. + Partner with supplier & internal SMEs to design and conduct experiments for process optimization and/or improvement. + Appropriately document experiment plans and results, including protocol writing and reports. + Partner with supplier & internal customers to ensure effective process control and monitoring of supplied material CTQ parameters and specifications Complete work order documentation.. + Partner with supplier & internal SMEs to implement various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing)Perform quality checks. + Lead the investigation, resolution and prevention of supplier related product and process nonconformance. + Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Supplier Quality function as a Core Team Member) + Troubleshoot equipment issues. + Lead in the completion and maintenance of supplier & component risk analysis. + Partner with internal customer and the supplier in the completion of component verification and validation. + Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. + Lead, coach, and mentor non-exempt and entry level exempt personnel + Performs other related duties and responsibilities, on occasion, as assigned. **EDUCATION AND EXPERIENCE YOU’LL BRING** **Required** + Bachelor's Degree in Engineering or Technical Field + Minimum 5 years of Engineering experience and demonstrated use of Quality tools/methodologies. + Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971. + Solid communication and interpersonal skills. + Strong project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner. + Advanced computer skills, including statistical/data analysis and report writing skills. + Experience implementing various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing. **Preferred** + Demonstrated supervisory experience preferred + Prior medical device experience preferred. + Experience working in a broader enterprise/cross-division business unit model preferred. + ASQ CQE or other certifications preferred Apply Now Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews. The base pay for this position is $72,700.00 – $145,300.00. In specific locations, the pay range may vary from the range posted. An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com