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