Position : Quality Engineer
Location : 9450 South State Street Sandy UT 84070 UNITED STATES
Duration : 12 +Months Contract
Qualifications:
Five years experience in Quality Engineering with emphasis on root cause and corrective action, continuous improvement, Six-Sigma tools and techniques and process validations.
• Auditing experience.
• Certification as an ASQ Certified Quality Engineer.
• Knowledge of document systems.
• Knowledge of lean manufacturing techniques preferred
Responsibilities:
• The Quality Engineer will be responsible for working closely with other functions within the organization (Manufacturing, R&D, Quality, Engineering, Procurement, Marketing) and ensuring the quality of the product and processes for the assigned product line(s) are in compliance with standard Quality practices.
• The QE will develop, modify, apply and maintain quality standards and protocols and may also be responsible for developing and implementing strategic quality plans, master validation plans, validation protocols, inspection plans and quality/regulatory compliance operating procedures to meet FDA (Food and Drug Administration) and ISO (International Organization of Standardization) requirements.
• Responsible for developing, documenting and/or maintaining design history files.
Location : 9450 South State Street Sandy UT 84070 UNITED STATES
Duration : 12 +Months Contract
Qualifications:
Five years experience in Quality Engineering with emphasis on root cause and corrective action, continuous improvement, Six-Sigma tools and techniques and process validations.
• Auditing experience.
• Certification as an ASQ Certified Quality Engineer.
• Knowledge of document systems.
• Knowledge of lean manufacturing techniques preferred
Responsibilities:
• The Quality Engineer will be responsible for working closely with other functions within the organization (Manufacturing, R&D, Quality, Engineering, Procurement, Marketing) and ensuring the quality of the product and processes for the assigned product line(s) are in compliance with standard Quality practices.
• The QE will develop, modify, apply and maintain quality standards and protocols and may also be responsible for developing and implementing strategic quality plans, master validation plans, validation protocols, inspection plans and quality/regulatory compliance operating procedures to meet FDA (Food and Drug Administration) and ISO (International Organization of Standardization) requirements.
• Responsible for developing, documenting and/or maintaining design history files.