Primary contact for engineering support of In-Process Inspectors. Support production efforts and process improvements (trend analysis, process validation, SPC). Coordinate In-Process MRB acitvities. Support Quality Systems (perform audits, SOP improvement, training, CAPA investigations). Ensure from the Quality prospective the transfer of new products from R&D to Production. Support Statistical Techniques and SPC interpretation. Present PPR and Management Review
Qualifications
2+ years of industry experience in ISO-9001 environment, preferably medical device. Bachelor of Science or higher degree in ME, IE or equivalent
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