Extrusion Manufacturing Engineer II

Abbott•Plymouth, MN

2d•$61,300 - $122,700•Onsite

About The Position

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 . Free medical coverage for employees via the Health Investment Plan (HIP) PPO 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. Main Purpose of the Role This position will design and develop manufacturing processes, tooling, and fixtures in order to meet daily production schedules while enhancing productivity and product quality.

Requirements

Bachelor's Degree (± 16 years) in Mechanical, Industrial, Chemical, Biomedical, or related Engineering area or an equivalent combination of education and work experience
Minimum 3 years of Manufacturing engineering experience required.
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 the ability to effectively communicate at multiple levels in the organization.
Multitasks, prioritizes, and meets deadlines in a timely manner.
Strong organizational and follow-up skills, as well as attention to detail.

Nice To Haves

Previous extrusion experience preferred.
Previous medical device experience preferred.
Experience working in a broader enterprise/cross-division business unit model preferred.
Ability to travel approximately 25%, including internationally

Responsibilities

Design and develop manufacturing processes, tooling, and fixtures in order to meet daily production schedules while enhancing productivity and product quality.
Evaluation of production equipment.
Production support and process validation.
Interface with vendors for incoming components.
Troubleshoot the 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.