Zimmer, Inc. Quality Sr Engineer II (513529) in Warsaw, Indiana

Job SummaryResponsible for gathering relevant, factual information and data in order to solve quality related problems. Resolve issues by identifying and applying solutions from acquired technical experience and guided precedents. Plan and lead projects by identifying and organizing activities into time dependent sequencing with realistic timelines. Work effectively/ productively with all departments by developing a team atmosphere. Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals.Principal Duties and ResponsibilitiesEvaluating new product design and establishing risk assessments for new products, following the procedures and guidelines set forth in the QMS Establishing quality plans for new product development Completing CAPAs, Issue Evaluations, Health Hazard Assessments in a timeline manner using appropriate risk based processes Monitoring performance of processes to a standards Applying ISO and QSR requirements to processes and procedures for Zimmer and outside suppliers; Working with suppliers on new product introduction to insure that quality and performance requirements are fulfilled Assisting Manufacturing, Sourcing and Development in the interpretation and application of regulations and product specificationsExpected Areas of CompetenceAbility to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.). Facilitates team efforts on quality engineering projects. Ability to deliver, meet deadlines and have results orientation. Able to communicate both orally and in written form to multiple levels of the company. Microsoft Office Suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, understanding of QSR/ISO regulations, design assurance, risk assessment, FMEA, and product testing methods, validation and verification activities, knowledge of measurement methods Knowledge of statistics, process control, and process capability Full working knowledge of all supporting department needs and capabilities, including the ability to discern when inaccurate information is supplied and offer ideas for how to correct it. Thorough knowledge base of existing Zimmer Biomet products and a basic understanding of competitive productsEducation/Experience RequirementsB.S. in engineering or an alternative Bachelors degree program with certification as a quality engineer (e.g. CQE). Certification as a quality engineer (e.g. CQE) or the Reliability Engineer Certification (CRE) granted through the American Society of Quality (ASQ) preferred. 5-7 years experience in a Quality Engineering role; Medical device strongly preferred, or an equivalent combination of education and experience. Combination of education and experience may be considered (in evaluating experience relative to requirements)Travel Requirements-Up to 20%Additional InformationEOE/M/F/Vet/DisabilityVEVRAA Federal ContractorEqual Opportunity Employerminorities/females/veterans/individuals with disabilities/sexual orientation/gender identity