JT408 - QUALITY ENGINEER II

• Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
• Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
• Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
• May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
• Ensures that all process improvements and flow enhancements meet stringent requirements for the medical device manufacturing industry.

• Bachelor's in Industrial, Manufacturing, Mechanical, Electrical or Chemical Engineering
• 2+ years of relevant experience
• Experience with agile, flow acceleration, lean manufacturing concepts and transformations
• Experience in equipment & process validation
• Experience in cost analysis
• Project management and analytical problem-solving skills
• Fully bilingual (English/Spanish)
• Availability for 1st shift (40 hours per week)

Quality Consulting Group