Sr. Quality Engineer

Job DescriptionWorking 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 you dream of.An excellent retirement savings plan with high employer contribution.Tuition reimbursement, the student debt program and 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 OpportunityIn Abbott's Electrophysiology (EP) business, we're advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.We have an opening for a Sr. Quality Engineer at our Minnetonka, MN site within our Electrophysiology division. This position will provide Process/Quality Engineering support to manufacturing for commercially released product, helping to ensure delivery of highest quality product to the customer.What You'll Work OnReduces and controls manufacturing process defects (scrap, nonconforming material, customer complaints) by leading efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions.May be responsible for implementing product stops & documenting release criteria.Develops and implements product quality plans, documents and systems by creating product specifications, quality specifications, quality plans, risk analyses, FMEAs in conjunction with other product development team members.May be responsible for risk analyses and FMEAs.Develops and implements Process Monitoring Systems by identifying critical process steps which could culminate in possible sources of manufacturing defects and devising methods to reduce process variation in order to reduce/eliminate the cause of defects.Collects and analyzes Lead Manufacturing process defect data Product/Process improvement efforts (e.g. scrap, nonconforming product, customer complaints) by systematically gathering quality metric data and performing the appropriate analysis method(s) to enhance sustaining product design and new product development.Creates Quality Tools & Training Materials by applying body of knowledge/expertise and communicating to respective teams.Participates in the development of less experienced staff by setting an example, providing guidance and work direction, and offering counsel. May lead a project team.Participates in determining goals and objectives for projects. Influences middle management on technical or business solutions.May interact with vendors.Plans and organizes non-routine tasks w/approval. Initiates or maintains work schedule.Establishes priorities of work assignments.Exercises judgment in selecting innovative, practical methods to achieve problem resolution.Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources.Required QualificationsBachelors Degree5+ years of related experienceExperience with CAPAs and non conformance processesKnowledge of quality requirements within medical devices or similar regulated industryThe base pay for this position is $75,300.00 – $150,700.00 In specific locations, the pay range may vary from the range posted.Job Family:Operations QualityDivision:EP ElectrophysiologyLocation:United States > Minnesota > Minnetonka : 14901 DeVeau PlaceAdditional Locations:Work Shift:StandardTravel:NoMedical Surveillance:Not ApplicableSignificant Work Activities:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.