St. Paul, Minnesota, USA
1 day ago
Manufacturing Process Engineer II

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.

Manufacturing Process Engineer II

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 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 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 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 St. Paul, MN location in the Electrophysiology division. In 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.

As the Manufacturing Process Engineer II you will support manufacturing sustaining engineering, and operations projects. This position will be responsible for manufacturing processes and production and service activities through cross-functional projects aimed at enhancing productivity, cost and product quality. Product lines supported are comprised of electronic systems used in Electrophysiology to better the lives of patients around the globe.  The successful candidate will have experience with electronics and electronic assemblies in a medical device manufacturing setting. 

What You’ll Work On

Lead or serve as member on cross-functional project teamsInterfaces with Quality and Research and Development organizations to integrate new products or processes into the existing manufacturing area.Establish processes and compliance to design based on product specifications and requirementsEvaluate process and production equipment and design alternatives based on “Design for Manufacturability” principlesManage manufacturing compliance with Quality Control requirements (i.e., Design Control, Process validation etc.)Possess a strong understanding of medical device product lifecycle and change management process and requirementsPlans and organizes project assignments of substantial variety and complexity. Initiates or maintains schedule for projects and project milestones. Establishes priorities of individual or project assignments.Drive root cause corrective actions to manufacturing process and equipment using understanding of electronics, software, circuits and systemsInterface with vendors for incoming components, and assess manufacturing impact from design change projectsDesign, develop and sustain manufacturing processes, in order to meet daily production schedules while enhancing productivity and product qualityIdentify and execute cost reduction activitiesProduction support and process validationUnderstand Lean manufacturing concepts like Value Stream mapping, 5S and Visual Workplace to improve quality, labor efficiency, and throughput.Generate and modify manufacturing process documentationSupport all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.  Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.Performs other related duties and responsibilities, on occasion, as assigned

Qualifications

Bachelors of Science degree in Electrical or Mechanical Engineering, a related field or equivalent2-3 years of relevant engineering experienceDemonstrated experience with electronic hardware or software systemsStrong verbal and written communications with ability to effectively communicate at multiple levels in the organizationMultitasks, prioritizes and meets deadlines in timely mannerStrong organizational and follow-up skills, as well as attention to detailAbility to travel approximately 5%, including internationally

Preferred Qualifications

Experience working in a broader enterprise/cross-division business unit model preferred

Experience working in medical device or other regulated industry

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 and @AbbottGlobal



The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted.

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