The Quality Engineer is responsible for coordinating medical device customers’ needs and requirements, as well as handling Major Quality Miscue (MQM) forms.
ESSENTIAL DUTIES AND RESPONSIBILITIES
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
** is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee. Other duties, responsibilities, and activities may change or be assigned at any time with or without notice. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.**
REPORTING RELATIONSHIP(S):
Reports directly to the Quality Assurance Manager
Requirements
QUALIFICATION REQUIREMENTS
The requirements listed below are representative of the education, certifications, knowledge, skills, and/or abilities required.
Education / Experience
Knowledge, Skills, and Abilities
PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
WORKING CONDITIONS
The working conditions described here are representative of those an employee may be exposed to while performing job duties and responsibilities.

KEB America is a leading manufacturer of industrial automation products, including industrial PCs, HMIs, I/O modules, VFDs, servo and induction motors, integral gearmotors, and clutches and brakes.
KEB America employs 125 people and delivers full design, assembly, and manufacturing at its 150,000 sq. ft. (ISO 9001:2015 certified) facility in Shakopee, Minnesota.
KEB Automation KG is headquartered in Barntrup, Germany. It has four global production sites (Germany, U.S., China, and Japan), 10 subsidiaries, 30 sales and service centers, and 1,500+ worldwide employees.