Engineer Manufacturing 4484

Trelleborg Medical Solutions Litchfield MN is seeking a Manufacturing Engineer to join our team. 

In this position, the candidate would apply engineering theory and principles to ensure that the manufacturing process is developed and maintained using best practices. Address technical issues as they come up related to the role via plant metrics and quality system requirements. Be inquisitive to new technologies and how we scale them up. Utilize data to make decisions. Procure capital for projects.

As a Valued Trelleborg team member, you will enjoy:

• Greater opportunity for impact


• Competitive compensation


• Generous benefits package: Health, Dental Vision, STD, LTD, Life, 401K


• Paid time off


• Quarterly Bonus

Education Requirement:

• Bachelor’s Degree in Industrial, Manufacturing or Mechanical Engineering or related discipline or equivalent combination of education and experience.

Senior Level (including above):

• Lean Sigma Green or Black Belt certification


• Polymer Science

Responsibilities:

• Analyze product specifications and translate these into manufacturing processes to establish production rates, achieve expected quality levels and establish reliability of finished product.


• Develop manufacturing methods for new and existing products, establish labor standards and develop product cost information.


• Meticulously document all manufacturing process information and sequences within the company document control system.


• Identify opportunities for improvement to existing processes and methods using data or observation. Develop the improvements and implement them as quickly as practical. 


• Make improvements to production rates and reduce scrap by identifying and implementing new and better equipment, processes or human factors methods.


• Assist production in troubleshooting production problems with individual components, individual processes and help improve the situation to assure customer delivery dates and superior quality.


• Strategize to resolve production problems.


• CAPA- Active member of the CAPA team responsible for implementing permanent corrective actions.


• NCMR- Participate in determination of product MRB disposition plan and approval with the MRB team.


• Follow ISO 13485 Quality System protocols.


• Execute engineering studies and projects. Record data and observations to analyze and make decisions on performance and quality requirements.


• Actively Support Production, Engineering and Quality departments.


• Work safely and act in accordance with all safety policies and procedures.


• Collaborate with Tool Room, and Training departments as needed.


• Other duties as assigned.