12 months contract to start with
The Quality Engineer will be supporting Change Control, in an ISO 13485 and FDA regulated medical device work environment. In this role he/she will interface with R&D, Engineering and Operations to ensure the successful implementation of changes. This might include changes to parts, products, and/or processes.
Education: BS/BA in Engineering (or advanced degree) or equivalent combination of education and experience.
Working experience in a regulated, Medical Device environment. Experience gathering and analyzing quality data for trending purposes using software tools such as MiniTab and Microsoft Excel. Preparation of QA reports.
Experience working directly with Geometric Dimensioning and Tolerancing (GD&T) and with Incoming Inspection practices