Engineer, Manufacturing II
AbbottAbout the role
JOB DESCRIPTION:
Manufacturing Engineer II
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
This position works out of our Plymouth MN location in the Electrophysiology Medical Device 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.
We are seeking an experienced, high caliber Manufacturing Engineer II for our Manufacturing area. This position will provide engineering support to existing manufacturing processes, tooling, and fixtures to meet daily production schedules while improving productivity and product quality.
What You'll Work On
Support and continuously improve manufacturing processes, tooling, and fixtures to meet daily production schedules while enhancing productivity and product quality.
Production support and process validation.
Support Supply Chain Resilience efforts to implement supply chains as necessary
Troubleshoot manufacturing process and equipment.
Utilize tools like DMAIC, 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.
Lead project efforts within Safety, Quality, Delivery, Cost priorities (example: CAPA ownership)
Generate and modify manufacturing process documentation.
Work with cross functional and dual site manufacturing teams
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.
Required Qualifications
Mechanical, Industrial, Chemical, Biomedical or related Engineering are
Minimum 4 years Manufacturing engineering experience required. Previous regulated manufacturing environment experience preferred.
Experience working in a broader enterprise/cross-division business unit model preferred.
Ability to work in a highly matrixed and geographically diverse business environment.
Ability to work within a team and as an individual contributor in a fast-paced, changing environment
Ability to leverage and/or engage others to accomplish projects.
Strong verbal and written communications with ability to effectively communicate at multipl
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