Demant Operations, S.A. de C.V.

Senior Manager Operations Quality

Demant Operations, S.A. de C.V.

Tijuana, Baja California

Mayo 27 2025

Compartir:

Giro

Manufacturera

Actividad principal

Manufactura de aparatos auditivos

Número de empleados

750

Datos de sucursal

Boulevard Corredor Tijuana-Rosarito 2000 #24702 Int H1 Ejido Francisco Villa Tijuana, Baja California

Descripción y detalle de las actividades

You will be responsible for developing, implementing, maintaining, and measuring the effectiveness of the quality system (inspection systems, policies and procedures, measurement and testing, corrective actions, internal and external audits, etc.) that was established to ensure that the product meets both internal and external quality standards.


DUTIES AND RESPONSIBILITIES

  • Production and distribution product quality matters
  • For setting Quality KPI's for production and distribution.
  • For calling and managing TJ production stop in coordination with VP Global Operations Quality.
  • For ensuring continuous alignment of learning and ways of working across sites.
  • For compliance with production and distribution standards in Demant, following QMS TJ.
  • For compliance with quality standards in Demant following QMS– TJ.
  • For compliance with regulatory standards in Demant Following QMS– TJ.
  • For creating and maintaining the yearly budget process. (Budget vs Actual balance)
  • For planning training for quality employees.
  • For providing input for Management Review according to HIQMS.
  • CAPA approver and QA Representative.
  • Validation approver.
  • For efficient allocation of quality resources, ensuring optimal operational engagement.
  • Driving the Quality requirements and awareness in Tijuana.
  • Proactively following the escalation model in case of any adverse events.
  • Local Quality Management System Representative on behalf of Global Quality
  • For coordination of activities related to maintaining and improving the quality management system.
  • For supervision of the corrective and preventive actions.
  • For preparation and hosting external audit (Customer, Notified Body).
  • For being compliance with and steer the Internal audit plan.

Experiencia y requisitos

We are looking for a candidate with a strong track-record within the Quality function combined with broad experience and Regulatory Compliance. You should have a solid conceptual and hands on understanding of Site Operations and how they are best executed in a global organization.

The qualifications required for this role are the following:

  • Engineering degree
  • Work experience in Medical Devices as Quality Manager.
  • Demonstrated leadership and supervisory experience.
  • Problem solving techniques (5whys, 8Ds, Ishikawa, DMAIC).
  • Effective organizational and communications – Fully bilingual (Spanish and English)
  • Strong Stakeholder management.


Beneficios

  • seguro de vida
  • comedor
  • fondo de ahorro
  • transporte
  • uniforme
  • gimnasio
  • seguro de gastos médicos
  • Beneficios de acuerdo a la LFT

Número de vacantes 1

Área Calidad

Contrato Permanente

Modalidad Presencial

Turno Diurno

Jornada Tiempo Completo

Horario
  • Tiempo completo

Estudios Carrera con título profesional

Inglés Hablado: Avanzado, Escrito: Avanzado

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