Quality Engineer

at  Katalyst Healthcares Life Sciences

Responsibilities:

• Support the initiatives of the Quality Assurance department
• Supply chain support in the development and maintenance of a supplier rating system and supplier evaluation
• Develop and provide statistical analysis of quality performance, problems and recommend solutions to both legacy and new products
• Support the implementation of a Statistical Process Control environment
• Support continuous improvement activities geared towards elimination of processes variation, nonconformities and cost reduction
• Perform internal ISO audits of the processes and activities throughout the organization and prepares respective audit reports.
• Provide monthly/daily reports and analysis as requested
• Develop control plans, check lists, and inspection procedures for new and existing products
• Train CNC personnel on inspection techniques
• Develop gauging requirements for new and existing products
• Active participation in Material Review Board (MRB) activities
• All other tasks are assigned by department management

Requirements:

• Bachelor’s Degree in Quality, Mechanical, or Industrial Engineering or High School Diploma or G.E.D.
• Demonstrable track record over a minimum of 5 years of successfully working in a fast-paced manufacturing environment.
• Familiarity of Six Sigma.
• Display ISO knowledge.
• Strong project management experience.
• Cross functional team builder/player with high levels of professionalism, integrity, and enthusiasm.
• Must have senior management potential/interest.
• Knowledge of Microsoft office (word and excel) and Minitab.
• Excellent communication skills both verbal and written.
• Required CMM (Coordinate Measuring Machine) experience.

• Support the initiatives of the Quality Assurance department
• Supply chain support in the development and maintenance of a supplier rating system and supplier evaluation
• Develop and provide statistical analysis of quality performance, problems and recommend solutions to both legacy and new products
• Support the implementation of a Statistical Process Control environment
• Support continuous improvement activities geared towards elimination of processes variation, nonconformities and cost reduction
• Perform internal ISO audits of the processes and activities throughout the organization and prepares respective audit reports.
• Provide monthly/daily reports and analysis as requested
• Develop control plans, check lists, and inspection procedures for new and existing products
• Train CNC personnel on inspection techniques
• Develop gauging requirements for new and existing products
• Active participation in Material Review Board (MRB) activities
• All other tasks are assigned by department managemen