Manufacturing Engineer

*Imagine leveraging your engineering expertise while working for one of the leading contract manufacturers in the world. Seize this rare opportunity to be part of a healthcare and medical business unit with the support and stability of an organization that has been in business for over 100 years!* Trelleborg Medical Solutions is seeking a **Manufacturing Engineer** to join their team in Delano, MN. Follows good manufacturing practices (GMP) and principles to provide engineering support and develop robust manufacturing processes. Has a primary role in the engineering of new, modified and/or existing manufacturing operations in a clean-room environment. Apply engineering theory and principles to ensure that the Value Stream for specific products is optimized using Lean Sigma tools. **Responsibilities:** - Analyze product specifications and translate these into manufacturing processes to establish production rates, achieve expected quality levels and establish reliability of finished product. - Identifies tooling related issues and communicates/works with a tool maker to resolve the issues - 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 Trelleborg 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. - Review production schedules and engineering specifications to resolve production problems. - CAPA- Active member of the CAPA team responsible for implementing permanent corrective actions. - DMR- Participate in determination of product DMR disposition plan and approval with the VS team. - Follow ISO 13485 and 21 CFR part 11 and part 820 and Trelleborg Quality System protocols. - Execution of DOE's, problem solving, FMEA's, validations, control plans, continuation engineering for products. - Actively Support Production, Engineering and Quality departments. **Education and Experience Requirements:** - Bachelor’s Degree in Industrial, Manufacturing or Mechanical Engineering or related disciplinE Desired - Medical device manufacturing experience - injection molding experience **Competencies** - Ability to read, write, speak and understand the English language - Ability to communicate clearly by conveying and receiving ideas, information, and direction effectively - Ability to demonstrate adequate job knowledge to deliver a world-class performance - Ability to challenge oneself to consistently meet all goals and deadlines - Willingness to strive for excellence by producing work that is free of errors and mistakes - Desire to delight both customers and coworkers by offering encouragement, fostering teamwork and addressing conflict appropriately - Commitment to making improvements company-wide - Use of statistical analysis software - Interpersonal skills and good communication technique - Ability to coordinate multiple projects and deadlines, manage and identify the scope - Lean Manufacturing- Proficient in the use of problem-solving tools such as 5 why, Fishbone, 8D, etc. - Understanding of manufacturing processes for medical components and devices. - Good understanding of metrology principles and methods. **Salary Range** $75,000-95,000/year based on experience **As a valued team member with Trelleborg, you will enjoy:** - Competitive compensation: Plus, bonus opportunities! - Generous benefits package: Includes health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement,…