Manufacturing Engineer
AbbottAbout the role
JOB DESCRIPTION:
Job Title
Manufacturing 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 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
We are seeking a Manufacturing Engineer for our Vascular division in either St. Paul, MN. This role is fully onsite role.
Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.
Job Summary:
This position will be a sustaining engineering position supporting the FFR and OCT hardware portion of our business. Performs the layout, construction, and evaluation of a variety of prototype Printed Circuit Boards, fixtures, and tools. Applies engineering and scientific principles to the evaluation and solution of technical problems. Exercises technical judgment in planning, organizing, performing, coordinating and/or directing engineering work. Performs engineering studies. Remains abreast of and consults on technical advancements. Identifies and routinely uses the most effective and cost-efficient practices to execute processes; continually evaluates their effectiveness and appropriateness.
Job Duties:
- Support all sustaining activities around catheter manufacturing including end of life, supplier change requests, Global compliance standards, IFU/Label changes, support of regulatory submissions, corporate programs, literature review, and all supporting quality system elements
- The position will also support the following manufacturing elements:
- Production support and process validation
- Interface with vendors for components
- Troubleshoot manufacturing process and equipment
- Utilize tools like Gage R&R, Cp, Cpk, and SPC to improve processes
- Understand manufacturing concepts like Value Stream mapping, 5S and Visual Workplace to improve quality, labor efficiency, and throughput.
- Protocol and report writing
- Generate and modify manufacturing process documentation
- Work with cross functional teams as required
- Develop and implement process improvements
- Support 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.
Equipment:
Works with standard office equipment such as telephone, cellular phone, fax/copier, and a personal computer with standard office software.
- Knowledge of analog electronics
- Experience with fiber optics is beneficial
- Working knowledge of laser equipment is beneficial
- Capital equipment experience is preferred
Works primarily in a standard office environment with air conditioning, good lighting with a low to moderate noise level. May also visit research labs, testing labs,
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