Sr Quality Engineer

hace 6 meses

Mexicali, México Intuitive Surgical A tiempo completo
Company DescriptionDescripción de la empresa

En 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

Roles & Responsibilities:

 

  • Initial Roles and responsibilities for this position has responsibility will include the following: 50% involvement in supporting manufacturing operations, 25% in product changes or new product introduction projects, 15% failure investigation, 10% preforming complex inspection and project management.
  • Develop and apply corporate level quality metrics.
  • Support line transfers between Intuitive buildings and regions.
  • Product Development- Handle projects of various product and subsystem types (Instruments, Accessories, 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 knowledge.
  • Ensure 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 Analysis- Provide 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 failure.
  • Review 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

Skills, Experience, Education, & Training:

 

  • Minimum Education: bachelor’s degree in electrical, mechanical or system engineering, math, or physics. Advanced degree preferred.
  • Proficient in English. Ability to communicate efficiently is a must.
  • Minimum 8+ years of working experience in Quality Engineering, or in manufacturing environment, minimum 4 years in medical device design or manufacturing environment.
  • Understands Quality and compliance System.
  • Understands of CFR 21 Part 820/ ISO 13485 requirements for making process or design changes.
  • Has a good grasp of risk assessments (Clinical/Usability risk assessments, FMEAs, etc.).
  • 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 (e.g., 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
  • Personality Requirements: able to cope with changes and uncertainties; and handle associate risks comfortably.
  • Ability to bring unpleasant facts to discussion, does not hold back information.
  • Results driven.
  • 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.

 

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.

Shift: Day
Travel: 25% of the time

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