Supplier Quality Engineer - Tijuana, México - BAXTER

BAXTER
BAXTER
Empresa verificada
Tijuana, México

hace 2 semanas

Rodrigo Fernández

Publicado por:

Rodrigo Fernández

Reclutador de talento para beBee
Descripción

This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world.

You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.


RESUMEN - JOB SUMMARY:
Esta posición participa en la calidad del proveedor relacionada con el monitoreo y la mejora del desempeño proveedor. Coordina la resolución de problemas de calidad de partes suministradas. This position participates in supplier quality related to monitoring and improvement of supplier performance. Coordinates problem solving from parts supplied.

ACTIVIDADES PRINCIPALES Y RESPONSABILIDADES - ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Planificar, coordinar, programar, ejecutar auditorías de proveedores a nível nacional e internacional según sea necesario. Plan, coordinate, Schedule, execute supplier audits domestically and internationally as required.
  • Seguimiento de las auditorías de los proveedores para demostrar los controles de los proveedores requeridos por FDA CFR 820, ISO 13485 e ISO 9000. Follow up on supplier audits to demonstrate supplier controls required by FDA CFR 820, ISO 13485 and ISO 9000.
  • Trabaja con personal de abastecimiento para coordinar las actividades de auditorías de proveedores según sea necesario. Work with sourcing staff to coordinate supplier audits activities as required.
  • Desarrolla técnicas de inspección, prueba y evaluación de partes. Develops inspection and test techniques to evaluates supplier materials.
  • Trabaja con proveedores para encontrar acciones a los problemas que se identifiquen. Works with suppliers to find solutions to identified problems.
  • Crear reportes escritos y comunicar los resultados de manera clara y eficaz al auditado y la gerencia de Welch Allyn. Create written reports and communicate the results clearly and effectively to the auditee and Welch Allyn management.
  • Gestionar y asegurar la implementación oportuna de los informes de acción correctiva del proveedor (SCARs). Manage and insure timely implementation of supplier Corrective Action Reports (SCARs).
  • Proporcionar soporte de ingeniería para problemas de material no conforme (NMR) y autorización de devolución de materiales (RMA). Provide engineering support for nonconforming material (NMR) and Return Material Authorization (RMA) issues.
  • Corregir los archivos de proveedores para apoyar la actividad de desarrollo actual y de negocio relacionada con la adquisición de nuevos negocios. Remediate Supplier files to support current and business development activity related to acquisition of new businesses.
  • Verifique que los archivos de proveedores se mantengan y documenten apropiadamente. Verify supplier files are maintained and documented appropriately.
  • Proporcionar métricas de proveedores a la gerencia. Provide supplier metrics to management.
EDUCACIÓN EXPERIENCIA, CERTIFICACIONES Y HABILIDADES - EDUCATION, EXPERIENCE, QUALIFICATIONS AND SKILLS:

Educación requerida - Education required:
Carrera en Ingeniería Requerida. B.S Degree in Engineering required.

Experiência Deseable: 3 años de experiência, incluyendo experiência previa con auditorías de calidad, específicamente auditorías de proveedores. Excelente documentación, comunicación y habilidades de resolución de problemas.

Conocimiento de los requisitos de FDA CFR 820, ISO 13485 e ISO 9000, altamente deseable contar con certificación de auditor líder ISO 13485.

Desirable Experience: 3 year qualifying experience, including previous experience with quality auditing, specifically supplier audits. Excellent documentation, communication and problem-solving skills desirable. Knowledge of FDA CFR 820, ISO 13485 and ISO 9000 requirements, strongly desired ISO 13485 Lead Auditor certification.

Bilingüe:
Comunicaciones orales y escritas en inglés y español requerido.

Bilingual:
Oral and written communications in English and Spanish Required.


Reasonable Accommodations

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