Intuitive Surgical, S. de R.L de C.V.

Quality Engineer

Intuitive Surgical, S. de R.L de C.V.

Mexicali, Baja California

Enero 21 2026

Compartir:

Giro

Maquiladora (Export.)

Actividad principal

Productos médicos para cirugía.

Número de empleados

4500

Sitio Web corporativo

Datos de sucursal

Calzada Presidente Venustiano Carranza #1745 Colonia Calles Mexicali, Baja California

Descripción y detalle de las actividades

  • This position has responsibility and authority for: 50% involvement in new product development, 25% failure investigation, 25% quality advocacy and project management.
  • Quality Advocacy and Project Management- Develop and apply corporate level quality metrics.

Product Development- Handle projects of various product and subsystem types (System, Software, Hardware, Mechanical, Vision, new products, product improvements, etc).

  • Work with product development teams to develop measurable goals for quality. Participate in the risk management process ensuring that the essential performance aspects are correctly mitigated in the product quality plans
  • Identify critical elements of designs based on design details and data-driven review of past designs. Recommend design processes and methods to meet quality goals: DFX, etc.
  • Work with the design teams to co-design robotic systems to enable self- diagnostic capabilities.
  • 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 Sunnyvale, 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

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.

Experiencia y requisitos

Skills, Experience, Education, & Training:

  • English Level: High Demonstrated interest in medical devices, and the medical field Bachelor’s degree in Engineering or Life Sciences Demonstrated understanding of medical device QMS requirements and regulatory requeriments, including but not limited to FDA CFR 21 820 and ISO 13485
  • Minimum Education: Minimum degree in electrical, mechanical or system engineering, math, or physics. Advanced degree preferred.
  • At least two areas of deep technical expertise applicable to the manufacture of medical robotic systems. A minimum of 5 years’ experience in one of these disciplines and a few years in a second discipline. Example areas of expertise:- Quality science and quality management
  • Quality statistics
  • Medical device software development, software quality best practices
  • Controls, algorithm development
  • Mechanical engineering, with experience relevant to robotic systems
  • Electrical engineering, with experience relevant to robotic systems
  • Design for reliability, manufacturability, serviceability
  • Proven ability to work in teams and to project-manage cross-functionally
  • Strong interpersonal and communication skills
  • Ability to influence others:
  • Passionate about our mission to improve product quality
  • Able to use persuasive, logical arguments based on data
  • Demonstrated understanding of product development lifecycles, design change and document change control, process verification and validation methodologies, production process control methodologies in a medical device environment
  • Previous work experience with product design changes, process verification and validation, as well as production process controls methodologies in an FDA/ISO regulated environment Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role.

Beneficios

  • seguro de vida
  • bonos anuales
  • caja de ahorro
  • comedor
  • fondo de ahorro
  • seguro de gastos médicos
  • servicios médicos en planta
  • Seguro dental
  • Acciones de la compañía
  • Becas educativas
  • Nutriológo
  • Clases de Yoga

Número de vacantes 1

Área Calidad

Contrato Permanente

Modalidad Presencial

Turno Diurno

Jornada Tiempo Completo

Horario
  • monday to friday 7.00 am - 4.30 pm

Estudios Carrera con título profesional

Inglés Hablado: 90%, Escrito: 90%

Disponibilidad p. viajar Si