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JABIL

Supplier Quality Engineer II

JABIL

  •  Expira 11/06/2026
  •  República Dominicana
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Detalle de la Oferta

Área de la Empresa Manufacturas Varias
Cargo Solicitado Asistente de Mantenimiento
Puestos Vacantes 1
Tipo de Contratación Tiempo completo
Nivel de Experiencia Sin experiencia
Salario máximo (USD)
Salario minimo (USD)
Vehículo Indiferente
País República Dominicana
Departamento Otro

Descripción de la Oferta

SUMMARY

Global support for supplier development and parts qualifications across Jabil Healthcare manufacturing locations. Ensures suppliers compliance with regulations and industry requirements. Assess supplier performance and risks as per Jabil's procedures.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

- Ensure that all production critical supplier issues are resolved in a timely manner, and corrective actions are implemented correctly.
- Support component/part qualification and risk assessment program.
- Support supplier selection strategies that will yield a supply base that can be used across all customer programs providing leverage cost savings.
- Proactively communicate information or issues that may impact the product costs of manufacturability to all affected departments.
- Technical escalation support in resolving supplier/component technical issues resulting in supplier corrective actions.
- Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor.
- Work or support cross-functional teams to improve customer metrics to ensure customer satisfaction both external and internal, and meet all regulatory requirements.
- Provide support to all Safety, Health and Environment (EHS) programs and initiatives to support our zero-accident culture.
- Comply and follow all procedures within the company security policy.
- May perform other duties and responsibilities as assigned.

EDUCATION & EXPERIENCE REQUIREMENTS

- Bachelor's degree in Mechanical, Manufacturing, Industrial Engineering preferred.
- At minimum of 2 to 4 years of experience in Quality or Engineering (regulated industries preferred); or equivalent combination of education and experience.
- Proficiency in use of Microsoft Office products (Excel, Word, Power Point, Visio, and Project).
- English proficiency (written / spoken)
- Experience working in ISO / FDA regulated industry preferred. .

OTHER REQUIREMENTS

- Ability to use statistical analysis software such as Minitab; would be preferred.
- Ability to work independently and with all stakeholders.
- Be familiar with the six sigma tools and method, basic statistic, ANOVA, FMEA/QCP, MSA, DOE, sampling plan, SPC, DMAIC/8D problem solving methodology, and APQP/AQP, etc.
- Must be able to read and interpret mechanical drawings. Must be experienced with reading and using Geometric Dimensioning and Tolerancing (GD&T).
- Must be able to execute Risk Assessments.
- Familiarity with SAP would be preferred.
- Team player, able to facilitate collaboration.

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