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

Analyst, Complaints

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

Tijuana, Baja California

Julio 01 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

Descripción de puesto

JOB SUMMARY:

This position will conduct product complaint evaluation, processing, and investigation for Hill-Rom products to support post market surveillance. The Associate Analyst, QA must be able to understand the customer’s allegation and accurately document the summary and investigation details as appropriate.

ESSENTIAL DUTIES AND RESPONSIBILITIES: – Other duties may be assigned and, as part of all job duties, employees are entrusted with a permanent mission of research and invention.

  • Manages complaint workflow and processes complaints within software applications.
  • Manages potentially reportable event workflow and processes potentially reportable events within software based on an understanding of the risks associated with product malfunction.
  • Ensures complaint records accurately reflect the allegation, investigation and conclusion of the customer complaint.
  • Works independently and with different parts of the organization to resolve complex issues.
  • Identifies the need for and requests engineering investigation reviews to identify the root cause for identified malfunctions.
  • Ensures timely closure of complaints to comply with regulatory requirements.
  • Adapts to changes in the work environment; manages competing demands; changes approach or method to best fit the situation; able to deal with frequent change, delays, or unexpected events.
  • Support internal corporate, notified bodies, third party, and regulatory audits as needed.

Experiencia y requisitos

EDUCATION, EXPERIENCE, QUALIFICATIONS AND SKILLS:

  • Associate degree or a minimum of 6 months to 1 year previous related work experience in the medical device or equivalent combination of education and experience.
  • Must be fluent in both speaking and writing in English.
  • Good written and verbal skills as well as good interpersonal, analytical and organizational skills.
  • Experience in resolving issues for internal and external customers.
  • Ability to work within deadlines, and work on multiple projects accurately and efficiently.
  • Some experience with QSR, Medical Device Directive, and ISO Quality System.
  • Ability to define problems, analyze data, establish facts and draw conclusions.
  • Attention to detail and accuracy is required.
  • Ability to function as an individual contributor within a team.
  • Proficiency with Microsoft Office Products such as Word, Excel or equivalent software. Familiarity with EtQ software is preferred.

Bilingual: Oral and written communication in English advance.

Beneficios

  • Beneficios de acuerdo a la LFT

Número de vacantes 4

Área Calidad

Contrato Temporal

Modalidad Presencial

Turno Diurno

Jornada Tiempo Completo

Estudios Carrera con título profesional

Inglés Hablado: Avanzado, Escrito: Avanzado

Disponibilidad p. viajar No