Baxter Healthcare - Welch Allyn de Mexico, S. de R.L. de C.V.

Eng. Supplier Quality

Baxter Healthcare - Welch Allyn de Mexico, S. de R.L. de C.V.

Tijuana, Baja California

Julio 30 2026

Compartir:

Corporativo

Giro

Maquiladora (Export.)

Actividad principal

Manufactura de instrumental médico de diagnóstico.

Número de empleados

990

Sitio Web corporativo

Datos de sucursal

*****@baxter.com

Emilio Flores 2471-A Cañon Del Padre Blvd. Teran Teran Tijuana, Baja California

Descripción y detalle de las actividades

Your role at Baxter:

This position participates in supplier quality related to monitoring and improvement of supplier performance. Coordinates problem solving from parts supplied.

Your team:

From your role as Sr Eng, Supplier Quality #This is where we count on your knowledge and talent to be responsible for planning, coordinating, scheduling and executing supplier audits nationally and internationally ensuring supplier quality in manufacturing processes at Baxter.

What you’ll be doing:

  • Plan, coordinate, Schedule, execute supplier audits domestically and internationally as required.
  • Follow up on supplier audits to demonstrate supplier controls required by FDA CFR 820, ISO 13485 and ISO 9000.
  • Work with sourcing staff to coordinate supplier audits activities as required.
  • Develops inspection and test techniques to evaluate supplier materials.
  • Works with suppliers to find solutions to identified problems.
  • Manage and insure timely implementation of supplier Corrective Action Reports (SCARs).
  • Lead the supplier approval process by assessing manufacturing, Quality Systems capabilities and risks.
  • Manages personnel maintain and reduce the Incoming Inspection cycle time.
  • Establishes problem solving strategies and work with Manufacturing and Quality Engineers to reduce MRB inventory.
  • Perform component characteristic analysis to determine inspection status changes.

Experiencia y requisitos

What you’ll bring:

  • Degree in Engineering required.
  • Knowledge of FDA CFR 820, ISO 13485 and ISO 9000 requirements, strongly desired ISO 13485 Lead Auditor certification
  • English
  • Desirable experience: 3 years or more of experience.
  • previous experience with quality auditing, specifically supplier audits. Excellent documentation, communication and excellent problem-solving skills are desirable.

Beneficios

  • Beneficios de acuerdo a la LFT

Número de vacantes 1

Área Calidad

Contrato Permanente

Modalidad Presencial

Turno Diurno

Jornada Tiempo Completo

Estudios Carrera con título profesional

Inglés Hablado: Avanzado, Escrito: Avanzado

Disponibilidad p. viajar No