Quality Engineer 1

Education and Experience 
 
 Associate’s Degree in technology or equivalent program, or completion of a Technical School with at least two years of relevant experience or the equivalent in related work experience 
 
 Experience on Final Inspection related activities in a medical device manufacturing environment a must 
 
 
 Special Requirements/Certifications 
 Knowledge of requirements and regulations related to ISO 13485 
 Knowledge of requirements and regulations of FDA CFR for Medical Devices 
 
 Knowledge, Skills and Abilities 
 Must have the ability to lift up to 25 lbs as needed 
 working knowledge in GD&T 
 Proficient skills in SAP 
 Demonstrated attention to detail and accuracy 
 Must be able to effectively communicate with Engineering, Production personnel, Supplier Operations and Materials in order to communicate and resolve inspection issues 

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