QLTY & RELIABILITY ENGINEER II

TE Connectivity Alajuela, Costa Rica

Company

TE Connectivity

Location

Alajuela, Costa Rica

Type

Full Time

Job Description

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.

Job Overview

TE Connectivity's Quality and Reliability Engineering Teams analyze the ability of product and production systems to comply with customer and contractual requirements through established reliability factors. They design, recommend revisions and install quality control systems, develop and document analytical methods for establishing reliability of products and their components and conduct analysis on relative reliability with regards to cost, structure, weight, maintainability, facility of production, and availability of materials and equipment. Out teams develop, implement and monitor company environmental safety programs and policies to ensure compliance with federal, state, and local environmental, health and safety regulations and recommend corrective actions if necessary. They are responsible for policies and practices to comply with applicable government regulations and industry requirements related to product environmental compliance, the implementation and management of technical and testing standards and specifications, quality control and reliability programs governing materials, product and processes, resulting in the optimization of material and labor, as well as failure analysis, root cause, corrective action and customer communication.

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What your background should look like:

Educación:

• Licenciatura o bachillerato con énfasis en ciencias o ingeniería.
• Título que le acredite para el desempeño del puesto en áreas de Ingeniería o una disciplina equivalente.
• Certificación CQE/CSSBB deseable.

Experiencia profesional:

• Mínimo de 2 años de experiencia en roles de calidad dentro de la industria médica, con experiencia demostrable en liderazgo de proyectos de calidad.
• Profundo conocimiento de las normativas y estándares de calidad aplicables en la industria médica (ISO 13485, FDA QSR, etc.), con certificaciones profesionales en calidad (como CQE, Six Sigma Black Belt) preferidas.
• Fuertes habilidades de liderazgo y capacidad para influir y motivar a los equipos.
• Excelentes habilidades analíticas, de resolución de problemas y de gestión de proyectos.
• Habilidades sobresalientes de comunicación y negociación.
• Dominio de herramientas informáticas avanzadas y software de gestión de calidad.
• Capacidad para gestionar múltiples proyectos y prioridades en un entorno dinámico.
• Experiencia previa trabajando en dispositivos médicos u otro entorno regulado por la FDA.

Competencias y habilidades:

• Excelente comunicación y habilidades interpersonales.
• Nivel de inglés al menos C1, comunicación constante con Clientes y el Corporativo.
• Altamente organizado con gran capacidad para priorizar tareas y trabajar por iniciativa.
• Capacidad para evaluar la información recopilada a partir de la observación, la experiencia, el razonamiento y / o la comunicación. Demostración de claridad, precisión, juicio independiente y minuciosidad.
• Excelente atención al detalle y redacción de informes.
• Posibilidad de flexibilizar los horarios de trabajo y disposición a viajar según sea necesario (hasta un 10%).
• Habilidades analíticas y de resolución de problemas.
• Excelentes habilidades de comunicación oral y escrita.
• Capacidad para trabajar en equipo y colaborar efectivamente con diferentes departamentos.
• Dominio de herramientas informáticas relacionadas con la gestión de calidad y análisis de datos.

Competencies

Values: Integrity, Accountability, Inclusion, Innovation, Teamwork

Apply Now

Date Posted

11/19/2024

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