Quality Engineer
hace 3 semanas
Company Description
Descripción de la empresaEn Intuitive, estamos unidos detrás de nuestra misión: creemos que la atención mínimamente invasiva es la atención que mejora la vida. Mediante la inventiva y la tecnología inteligente, ampliamos el potencial de los médicos para curar sin limitaciones.
Como pioneros y líderes del mercado en cirugía robótica, nos esforzamos por fomentar un equipo inclusivo y diverso, comprometido con marcar la diferencia. Durante más de 25 años, hemos trabajado con hospitales y equipos de atención de todo el mundo para ayudar a resolver algunos de los desafíos más difíciles de la atención médica y avanzar en lo que es posible.
Intuitive se ha construido gracias a los esfuerzos de grandes personas de diversos orígenes. Creemos que las grandes ideas pueden provenir de cualquier lugar: nos esforzamos por fomentar una cultura inclusiva basada en la diversidad de pensamientos y en el respeto mutuo. Lideramos con inclusión y capacitamos a los miembros de nuestro equipo para que trabajen de la mejor manera y manifiesten su auténtica personalidad.
Las personas apasionadas que quieren marcar la diferencia impulsan nuestra cultura: los miembros de nuestro equipo se basan en la integridad, tienen una sólida capacidad para aprender, la energía para hacer las cosas, y aportan experiencias diversas del mundo real para ayudarnos a pensar de nuevas maneras. Invertimos activamente en los miembros de nuestro equipo para apoyar su crecimiento a largo plazo y así poder continuar avanzando en nuestra misión y alcanzar su máximo potencial.
Únase a un equipo comprometido a dar grandes pasos hacia delante para una comunidad global de profesionales de atención médica y sus pacientes. Juntos, avancemos en el mundo de la atención mínimamente invasiva.
Job Description
Initial Roles and responsibilities for this position has responsibility will include the following:
50% involvement in supporting design and manufacturing projects, 15% failure investigation, 10% performing complex inspection and 25% quality advocacy and project management.
Quality Advocacy and Project Management. Develop and apply corporate level quality metrics. Lead and project manage quality initiatives in one or more of these focus areas:Product QualityData QualityProcess Quality Production facility validation planning, execution, and for building, product, and process located in Mexicali, Mexico. Product DevelopmentHandle projects of various product and subsystem types (System, Instruments, Vision, new products, product improvements, etc).Plan and direct creation of quality standards, quality control, and quality assurance procedures, sampling plans, test methods, fixtures, and processes for finished devices manufactured at, ISI Mexicali, and OEM suppliers, utilizing clinical and engineering process compliance through the design and development of comprehensive procedures including work instructions, flowcharts, forms, templates, checklists, and other product or process related documentation, for recording, evaluating, and reporting quality data.Develop and implement methods and procedures for disposition of discrepant material.Provide support to commercial product manufacturing processes, including failure analysis, documentation review and approval, tooling qualification, and defect containments. Failure AnalysisProvide quality expertise post market release to the quality engineering support team to analyze the returned product.Perform deep technical failure analysis based on the physics of and interpret complex data analysis rooted in an understanding of our product hardware and software, the physics of failure, and the use conditions in the clinical / operating room environment.
Qualifications
Required Skills, Experience, Education, And Training:
Competency Requirements: To adequately perform the responsibilities of this position the individual must possess:
Requires a minimum of 5 years of related experience with a University degree; or 3 years’ experience and a Master's degree; or a PhD; or equivalent experience. Minimum 4+ years of working experience in Quality Engineering, or in manufacturing environment, minimum 2 years in medical device design or manufacturing environment. Understands Quality and compliance System. Understands of CFR 21 820/ ISO 13485 requirements for making process or design changes. Have good grasp of quality control and tools. Able to learn the product and process quickly and assesses defects’ impact to product. Understands root cause investigation process and able to initiate routine problem-solving investigations. Involved in Design and process improvement projects in the past. Able to review Qualification and Validation protocols. Understands manufacturing metrics. Understands basic Excel data analysis operations (, Pareto, charts, and trend). Able to work in various project teams as the Quality SME. Able to communicate work tasks to various project team members. Capable of Compiling data in format appropriate for presentation.Preferred Skills and Experience
Able to cope with changes and uncertainties; and handle associate risks comfortably. Ask questions and don’t stop at the first answer. Analyze deeply to ensure the solution is the most effective solution. Brings unpleasant facts to discussion, does not hold back information. Driven by results. Fully supports team decision, even if he/she disagrees with the decision. Listens and respects others. Demonstrates constructive work relationship with others in the organization. Sets priority and manages time wisely, capable of identifying the critical issues from the trivial issues. Sets individual goals aligning with the team goal.
Additional Information
Intuitive es un empleador que brinda igualdad de oportunidades de empleo. Proporcionamos igualdad de oportunidades de empleo a todos los solicitantes y empleados cualificados, y prohibimos cualquier tipo de discriminación y acoso, independientemente de su raza, sexo, condición de embarazo, orientación sexual, identidad de género, origen nacional, color, edad, religión, condición de veterano protegido o de discapacidad, información genética o cualquier otra condición protegida por las leyes federales, estatales o locales aplicables.
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