Quality Engineer- Medical Device Manufacturing

TekWissen provides a unique portfolio of innovative capabilities that seamlessly combines clients insights, strategy, design, software engineering, and systems integration. www.tekwissen.com  - Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers. - Develops and implements corrective/preventative action plans.  - Collects and analyzes data for gauge and product evaluation. - Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products. - Ensures that suppliers have necessary information and facilities to deliver quality products - Ability to deliver, meet deadlines and have results orientation. - Able to communicate both orally and in written form to multiple levels of the company. - Demonstrates characteristics of high potential for future development opportunities. - Microsoft Office Suite - Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs. B.S. in engineering or an alternative Bachelor’s degree program with certification as a quality engineer (e.g. CQE) plus 3 years experience in a Quality Engineering role, or an equivalent combination of education and experience. Certified Quality Engineer (CQE) preferred.