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Zimmer Biomet Spine, Inc Quality Manager (679819) - AMER21494-343787 in Westminster, Colorado

Job SummaryZimmer Biomet is a world leader in musculoskeletal health solutions. Our teammembers are part of a company with a heritage of leadership, a focus onshaping the future, and a mission dedicated to alleviating pain andimproving the quality of life for people around the world.The Quality Manager:Ensures complaint investigations are completed in a timely and compliantmanner.Provides technical and administrative guidance to Quality Assurance,Manufacturing, and suppliers of raw materials or finished medical devices.Assures product conformance to established requirements and standards throughappropriate inspection and test activities.Coordinates quality planning, inspection method development and defectprevention/corrective action processes for new and existing products.Identifies and solves product and process problems and supports variousoperational groups.Assists in the preparation and monitoring of the operating and capitalbudgets.Principal Duties and ResponsibilitiesDetermine and define quality assurance requirements from review of engineeringdrawings and/or specifications, industry standards, governmentspecifications or other applicable source documents.Formulate, write and maintain procedures, specifications and standards forthe quality control of Zimmer products including non-destructive testingmethods, gauge design and procurement, sampling and inspection methods andvisual acceptance standards.Manages customer complaint process to ensure complaint investigations arecompleted in a timely and compliant manner.Develop and administer effective data collection and reporting system to meetregulatory requirements and management information needs.Control further processing, delivery or use of nonconforming products untildeficiency or unsatisfactory condition has been corrected.Provides resources, including the assignment of trained personnel forperformance of work and assessment activities to meet requirements.Implement defect prevention strategies utilizing SPC/SQC principles andpractices.Expected Areas of CompetenceLead and motivate team members through feedback and stretch assignments.Establishes and maintains high levels of credibility.Collaborates effectively across the organization, leverages resources fromother parts of the organization to build commitment and achieve results.Interpret engineering drawings and specifications.Teamwork and customer focus oriented.Demonstrate ability in selecting, interviewing, training, coaching,motivate, discipline, and direct people.Must possess good writing skills and be familiar with both the scientific andvernacular vocabularies.Good knowledge of applicable government specifications, standards andregulations such as Quality System Regulation and ISO standards.Education/Experience RequirementsA minimum of a Bachelors Degree or equivalent (preferably in engineering ora related discipline) with a minimum of 6 years of industry work experienceinvolving quality functions is required; or an advanced degree, i.e.,Masters Degree, in a related discipline with a minimum of 4 years ofindustry work experience involving quality functions is required.Demonstrated experience in all aspects of modern quality control methods,such as nondestructive testing, metrology, statistical process control,quality cost accounting, applied statistics and inspection is requiredDemonstrated experience in dealing with representatives from the Food and DrugAdministration or other regulatory agencies is requiredA Quality Engineering certification is highly preferred (e.g., CQA,CQE, CQM, etc.).Travel RequirementsUp to 10%Additional InformationEOE/M/W/Vet/DisabilityAt Zimmer Biomet, we believe in The Power of Us, which means that we arestronger together. We are committed to creating an environment where everyteam member feels included, respected, empowered, and celebrated.As a Zimmer Biomet team member, you will share in our commitment toproviding mobility and renewed life to people around the world. This is why we