At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. Position Summary As a Quality Inspector you will be responsible for administering the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR, and other applicable regulatory standards. Quality Inspectors support manufacturing and servicing operations by performing incoming component and in-process product inspections using standard measurement equipment. They identify; segregate and document rejected material and participate in Material Review Boards to ensure the proper documentation and disposition. They may also reviewother related Quality documentation such as device history or calibration records. Shift: 3:00pm-1:30am Monday - Thursday (Will start on 1st shift for training and then move to 2nd shift)
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Job Type
Full-time
Career Level
Entry Level
Industry
Miscellaneous Manufacturing
Education Level
No Education Listed
Number of Employees
5,001-10,000 employees