Manufacturing Process Engineer

2 weeks ago


Litchfield, Minnesota, United States Trelleborg Group Full time
Position Overview:

Trelleborg Medical Solutions is seeking a dedicated Manufacturing Engineer to enhance our operational capabilities. This role is pivotal in applying engineering principles to ensure that our manufacturing processes are optimized and adhere to industry best practices.

Key Responsibilities:
  • Address technical challenges as they arise, utilizing plant metrics and quality system requirements.
  • Explore and evaluate new technologies for scalability.
  • Leverage data-driven decision-making to enhance manufacturing efficiency.
  • Manage capital procurement for engineering projects.
As a valued member of Trelleborg, you will benefit from:
  • Significant opportunities for impact.
  • Competitive salary and comprehensive benefits package, including Health, Dental, Vision, STD, LTD, Life Insurance, and 401K.
  • Paid time off and quarterly bonuses.
Educational Qualifications:

A Bachelor's Degree in Industrial, Manufacturing, or Mechanical Engineering, or a related field, or an equivalent combination of education and experience is required.

Preferred Qualifications:
  • Lean Sigma Green or Black Belt certification.
  • Knowledge in Polymer Science.
Responsibilities Include:
  • Analyzing product specifications and translating them into effective manufacturing processes to achieve production targets and quality standards.
  • Developing manufacturing methodologies for both new and existing products, establishing labor standards, and calculating product costs.
  • Documenting all manufacturing processes meticulously within the company’s document control system.
  • Identifying and implementing improvements to existing processes through data analysis and observation.
  • Enhancing production rates and minimizing waste by introducing innovative equipment and processes.
  • Assisting production teams in troubleshooting and resolving operational issues to ensure timely delivery and high-quality output.
  • Strategizing solutions for production challenges.
CAPA Responsibilities:
  • Actively participating in the CAPA team to implement permanent corrective actions.
NCMR Responsibilities:
  • Contributing to the product MRB disposition plan and collaborating with the MRB team.

Adhering to ISO 13485 Quality System protocols is essential. This role involves executing engineering studies and projects, recording data and observations to inform performance and quality decisions. You will also provide support to Production, Engineering, and Quality departments while ensuring compliance with safety policies and procedures. Collaboration with Tool Room and Training departments may be required as needed.

Other duties may be assigned as necessary.



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