Manufacturing Quality Engineer #ESF6880

• Our client is a global medical technology company that is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. 
  
  


• They are one of the largest global medical technology companies in the world.
  
  


• Its 65,000 employees have a passion and commitment to help improve patient outcomes, improve the safety and efficiency
  
  


• Career advancement, well liked management
  
  


• Autonomy in the workplace
  
  

What you will be doing:

• Act as a resource to work groups and project teams, within the plant and outside the plant, regarding quality and regulatory issues.
  
  


• Lead or participate on Kaizen teams to improve quality and reduce waste.
  
  


• Investigate and provide engineering solutions to quality-related manufacturing issues.
  
  


• Maintain familiarity with manufacturing processes and products to evaluate the cause and effect of defects and identify trends in process and product quality.
  
  


• Provide technical input for projects using FMEAs, risk mitigation, plant validations, DOE experiments, and other experiments and investigations as assigned.
  
  


• Lead projects using continuous improvement tools and methodologies such as Six Sigma, Lean, and others.
  
  


• Work with all departments to maintain the highest quality standards.
  
  


• Formulate, review, and implement policies and procedures related to product quality and process control as appropriate.
  
  


• Ensure all activities comply with government regulations (OSHA, EPA, FDA, ISO, etc.) and corresponding company policies/procedures, including activities and programs defined in the Quality Systems Manual for Broken Bow.
  
  


• Coordinate machine and process capability studies, analyze the data, and submit recommendations.
  
  


• Design and assist Production, Engineering, and the Division in completing new product/process evaluations, including Hazard Analysis.
  
  


• Coordinate communication between Division R&D and plant personnel on new products, product improvements, and product issues.
  
  


• Participate in Engineering and Production functions as required to achieve the overall objectives of the plant.
  
  


• Perform other duties as assigned, such as Internal Audits and PIR/CFI investigations.
  
  


• Support plant safety initiatives.
  
  

Experience you will need:

• BA/BS degree in Science, Engineering, or a related discipline.
  
  


• Medical device manufacturing experience preferred.
  
  


• Preferred 1–2 years of relevant experience; however, internships, co-op experience, and relevant engineering projects will also be considered.
  
  


• Strong communication and interpersonal skills, with the ability to work effectively across diverse teams.
  
  


• Flexible and adaptable, with the ability to support a variety of day-to-day responsibilities.