Our Client, a Medical Device and Healthcare company, is looking for a Senior Manufacturing Engineer for their Minnetonka, MN location. Responsibilities: + Design and develop manufacturing processes, tooling, and fixtures in order to meet daily production schedules while enhancing productivity and product quality. + List the significant/essential duties, tasks or responsibilities which employees in this position are actually required to perform. + Manage projects which include new production equipment, process improvements and cost reductions while supporting new product introductions. + Provide guidance to other engineers and technicians. + Provide technical mentorship to engineers and technicians Conduct Process FMEAs and Process Validations Improve product quality, labor efficiency, and throughput through the use of Lean manufacturing concepts Coordinate the design, procurement, build and debug of tooling, machinery and test equipment Work with Product Development to ensure Design for Manufacturability Individual should: Be innovative, resourceful, and work with minimal direction Have excellent organization, problem solving, communication, and team leadership skills Work effectively with cross-functional teams Other Duties: List any other important but non-essential and/or infrequent duties performed. + Support all Divisional initiatives as identified by divisional 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. Requirements: + Bachelors Degree (± 16 years) Mechanical, Chemical or any engineering or technical degree ☒ an equivalent combination of education and work experience + Minimum 5 years Manufacturing engineering experience, medical device experience required. + International manufacturing experience preferred. + Strong analytical, problem solving and project management skills. + Six Sigma certification preferred. + Demonstrated leadership capability in team settings. 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 multiple levels in the organization. Multitasks, prioritizes, and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail. Why Should You Apply? + Health Benefits + Referral Program + Excellent growth and advancement opportunities As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, gender, sexual orientation, gender identity or express, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws.